U.S. patent number 9,181,603 [Application Number 14/388,285] was granted by the patent office on 2015-11-10 for processes for treating fly ashes.
This patent grant is currently assigned to Orbite Technologies Inc.. The grantee listed for this patent is ORBITE ALUMINAE INC.. Invention is credited to Richard Boudreault, Joel Fournier, Denis Primeau.
United States Patent |
9,181,603 |
Boudreault , et al. |
November 10, 2015 |
Processes for treating fly ashes
Abstract
There are provided processes for treating fly ash. For example,
the processes can comprise leaching fly ash with HCl so as to
obtain a leachate comprising aluminum ions and a solid, and
separating the solid from the leachate; reacting the leachate with
HCl so as to obtain a liquid and a precipitate comprising the
aluminum ions in the form of AlCl.sub.3, and separating the
precipitate from the liquid; and heating the precipitate under
conditions effective for converting AlCl.sub.3 into Al.sub.2O.sub.3
and optionally recovering gaseous HCl so-produced.
Inventors: |
Boudreault; Richard
(St-Laurent, CA), Fournier; Joel (Carignan,
CA), Primeau; Denis (Ste-Julie, CA) |
Applicant: |
Name |
City |
State |
Country |
Type |
ORBITE ALUMINAE INC. |
St-Laurent |
N/A |
CA |
|
|
Assignee: |
Orbite Technologies Inc.
(St-Laurent, CA)
|
Family
ID: |
49257993 |
Appl.
No.: |
14/388,285 |
Filed: |
March 11, 2013 |
PCT
Filed: |
March 11, 2013 |
PCT No.: |
PCT/CA2013/000218 |
371(c)(1),(2),(4) Date: |
September 26, 2014 |
PCT
Pub. No.: |
WO2013/142957 |
PCT
Pub. Date: |
October 03, 2013 |
Prior Publication Data
|
|
|
|
Document
Identifier |
Publication Date |
|
US 20150075328 A1 |
Mar 19, 2015 |
|
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
Issue Date |
|
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61617422 |
Mar 29, 2012 |
|
|
|
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61706028 |
Sep 26, 2012 |
|
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|
Current U.S.
Class: |
1/1 |
Current CPC
Class: |
C22B
26/10 (20130101); C01F 17/224 (20200101); C01F
17/235 (20200101); C22B 26/22 (20130101); C01F
5/10 (20130101); A62D 3/36 (20130101); C01B
33/126 (20130101); C01F 7/306 (20130101); C22B
3/10 (20130101); C01F 5/30 (20130101); C22B
7/02 (20130101); C22B 21/0023 (20130101); C01G
49/06 (20130101); C22B 59/00 (20130101); C01F
7/22 (20130101); A62D 3/40 (20130101); C01D
1/04 (20130101); C01F 17/218 (20200101); C01F
7/56 (20130101); C22B 21/0007 (20130101); C01G
49/10 (20130101); A62D 2101/08 (20130101); Y02P
10/146 (20151101); Y02W 30/50 (20150501); Y02P
20/129 (20151101); Y02P 10/20 (20151101); A62D
2203/02 (20130101); Y02C 20/20 (20130101) |
Current International
Class: |
A62D
3/36 (20070101); C01G 49/10 (20060101); C01G
49/06 (20060101); C01B 33/12 (20060101); C01D
1/04 (20060101); C01F 17/00 (20060101); C01F
7/22 (20060101); C01F 5/30 (20060101); C01F
5/10 (20060101); C01F 7/56 (20060101); A62D
3/40 (20070101); C01F 7/30 (20060101); C22B
21/00 (20060101); C22B 3/10 (20060101); C22B
7/02 (20060101) |
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|
Primary Examiner: Wyszomierski; George
Assistant Examiner: McGuthry Banks; Tima M
Attorney, Agent or Firm: Bereskin & Parr
LLP/S.E.N.C.R.L., s.r.l.
Parent Case Text
CROSS-REFERENCE TO RELATED APPLICATIONS
The present application is a 35 USC 371 national stage entry of
PCT/CA2013/000218 filed on Mar. 11, 2013 and which claims priority
on U.S. 61/617,422 filed on Mar. 29, 2012; and on U.S. 61/706,028
filed on Sep. 26, 2012. These documents are hereby incorporated by
reference in their entirety.
Claims
What is claimed is:
1. A process for treating raw fly ash, said process comprising:
optionally a pre-leaching treatment that consists of reducing the
particle size of said raw fly ash; leaching said raw fly ash with
HCl so as to obtain a leachate comprising aluminum ions and iron
ions and a solid, and separating said solid from said leachate;
reacting said leachate with HCl so as to obtain a liquid comprising
iron ions and a precipitate comprising said aluminum ions in the
form of AlCl.sub.3, and separating said precipitate from said
liquid; and heating said precipitate under conditions effective for
converting AlCl.sub.3 into Al.sub.2O.sub.3 and optionally
recovering gaseous HCl so-produced.
2. The process of claim 1, wherein said fly ash is leached with HCl
having a concentration of about 25 to about 45 weight %.
3. The process of claim 2, wherein said process further comprises
recycling said gaseous HCl so-produced by contacting it with water
so as to obtain a composition having a concentration of about 25 to
about 45 weight % and using said composition for leaching said fly
ash.
4. The process of claim 1, wherein said fly ash is leached with HCl
having a concentration of about 25 to about 45 weight % at a
temperature of about 125 to about 225.degree. C.
5. The process of claim 4, wherein said fly ash is leached at a
pressure of about 4 to about 10 barg (about 400 KPag to about 1000
KPag).
6. The process of claim 5, wherein said process is effective for
avoiding producing red mud.
7. The process of claim 1, wherein said fly ash is leached with HCl
having a concentration of about 25 to about 45 weight % at a
temperature of about 160 to about 190.degree. C.
8. The process of claim 1, wherein said fly ash is leached with HCl
having a concentration of about 18 to about 45 weight %.
9. The process of claim 1, wherein said fly ash is leached with HCl
having a concentration of about 18 to about 45 weight % at a
temperature of about 125 to about 225.degree. C.
10. The process of claim 1, wherein said recycled gaseous HCl
so-produced is contacted with water so as to obtain said
composition having a concentration between 18 and 36 weight %.
11. The process of claim 1, wherein said process comprises reacting
said leachate with gaseous HCl so as to obtain said liquid and said
precipitate comprising said aluminum ions, said precipitate being
formed by crystallization of AlCl.sub.36H.sub.2O.
12. The process of claim 11, wherein during said crystallization of
AlCl.sub.36H.sub.2O, said liquid is maintained at a concentration
of HCl of about 25 to about 35% by weight.
13. The process of claim 12, wherein said crystallization is
carried out at a temperature of about 45 to about 65.degree. C.
14. The process of claim 11, wherein said process comprises heating
said precipitate at a temperature of about 350.degree. C. to about
500.degree. C. for converting AlCl.sub.36H.sub.2O into
Al.sub.2O.sub.3.
15. The process of claim 1, wherein said process comprises reacting
said leachate with HCl recovered during said processs and having a
concentration of at least 30% by weight as to obtain said liquid
and said precipitate comprising said aluminum ions, said
precipitate being formed by crystallization of
AlCl.sub.3.6H.sub.2O.
16. The process of claim 15, wherein said crystallization is
carried out at a temperature of about 45 to about 65.degree. C.
17. The process of process of claim 1, wherein said process
comprises converting AlCl.sub.36H.sub.2O into Al.sub.2O.sub.3 by
carrying out a calcination of AlCl.sub.3.6H.sub.2O, said
calcination comprising steam injection.
18. The process of process of claim 17, wherein said steam is
overheated.
19. The process of claim 1, wherein said fly ash is leached at a
pressure of about 4 to about 10 barg (about 400 KPag to about 1000
KPag).
20. A process for preparing aluminum, said process comprising :
optionally a pre-leaching treatment that consists of reducing the
particle size of raw fly ash; leaching said raw fly ash with HCl so
as to obtain a leachate comprising aluminum ions and iron ions and
a solid, and separating said solid from said leachate; reacting
said leachate with HCl so as to obtain a liquid comprising iron
ions and a precipitate comprising said aluminum ions in the form of
AlCl.sub.3, and separating said precipitate from said liquid;
heating said precipitate under conditions effective for converting
AlCl.sub.3 into Al.sub.2O.sub.3 and optionally recovering gaseous
HCl so-produced; and converting said Al.sub.2O.sub.3 into aluminum.
Description
TECHNICAL FIELD
The present disclosure relates to improvements in the field of
processes for treating industrial waste materials. For example, it
relates to processes for treating fly ash. For example, these
processes can be effective for extracting various materials from
fly ash such as alumina and various metal oxides, silica, and rare
earths, etc.
BACKGROUND OF THE DISCLOSURE
fly ash is one of the residues generated in combustion. It
comprises fine particles that rise with the flue gases. Ash which
does not rise is termed bottom ash. Fly ash material can solidify
while suspended in the exhaust gases and is collected by
electrostatic precipitators Of filter bags. Since the particles
solidify while suspended in the exhaust gases, fly ash particles
can be generally spherical in shape and range in size from 0.5
.mu.m to 100 .mu.m. Fly ash can comprise silicon dioxide
(SiO.sub.2) (which can be present in two forms: amorphous, which is
rounded and smooth, and crystalline, which is sharp, pointed and
hazardous); aluminium oxide (Al.sub.2O.sub.3 ) and iron oxide
(Fe.sub.2O.sub.3), Fly ashes can also comprise calcium oxide (CaO),
Fly ashes can also be highly heterogeneous. They can comprise a
mixture of glassy particles with various identifiable
components.
For example, fly ash can refer to ash produced during combustion of
coal. Depending upon the source and makeup of the coal being
burned, the components of fly ash vary considerably,
In the past, fly ash was generally released into the atmosphere,
but pollution control equipment mandated in recent decades now
require that it be captured prior to release. Fly ash is generally
captured by electrostatic precipitators or other particle
filtration equipment before the flue gases reach the chimneys of
coal-fired power plants, and together with bottom ash removed from
the bottom of the furnace is in this case jointly known as coal
ash. For example, in the US, fly ash can be generally stored at
coal power plants or placed in landfills. About 43 percent is
recycled,.sup.[3] often used to supplement Portland cement in
concrete production. However, some scientists have expressed health
concerns about this.
In the past, fly ash produced from coal combustion was simply
entrained in flue gases and dispersed into the atmosphere. This
created environmental and health concerns that prompted laws which
have reduced fly ash emissions to less than 1 percent of ash
produced. Worldwide, more than 65% of fly ash produced from coal
power stations is disposed of in landfills and ash ponds. The
recycling of fly ash has become an increasing concern in recent
years due to increasing landfill costs and current interest in
sustainable development. As of 2005, U.S. coal-fired power plants
reported producing 71.1 million tons of fly ash, of which 29.1
million tons were reused in various applications. If the nearly 42
million tons of unused fly ash had been recycled, it would have
reduced the need for approximately 27,500 acreft (33,900,000
m.sup.3) of landfill space.
There is thus a need for at least an alternative process for
treating, recycling and/or valorizing fly ash.
SUMMARY OF THE DISCLOSURE
According to one aspect, there is provided a process for preparing
alumina and optionally other products, the process comprising:
leaching an aluminum-containing material with HCl so as to obtain a
leachate comprising aluminum ions and a solid, and separating the
solid from the leachate; reacting the leachate with HCl so as to
obtain a liquid and a precipitate comprising the aluminum ions in
the form of AlCl.sub.3, and separating the precipitate from the
liquid; heating the precipitate under conditions effective for
converting AlCl.sub.3 into Al.sub.2O.sub.3 and recovering gaseous
HCl so-produced; and recycling the gaseous HCl so-produced by
contacting it with water so as to obtain a composition having a
concentration higher than HCl azeotrope concentration (20.2 weight
%) and reacting the composition with a further quantity of
aluminum-containing material so as to leaching it.
According to another aspect, there is provided a process for
preparing alumina and optionally other products, the process
comprising: leaching an aluminum-containing material with HCl so as
to obtain a leachate comprising aluminum ions and a solid, and
separating the solid from the leachate; reacting the leachate with
HCl so as to obtain a liquid and a precipitate comprising the
aluminum ions in the form of AlCl.sub.3, and separating the
precipitate from the liquid; heating the precipitate under
conditions effective for converting AlCl.sub.3 into Al.sub.2O.sub.3
and recovering gaseous HCl so-produced; and recycling the gaseous
HCl so-produced by contacting it with water so as to obtain a
composition having a concentration of about 18 to about 45 weight %
or about 25 to about 45 weight % and reacting the composition with
a further quantity of aluminum-containing material so as to
leaching it.
According to another aspect, there is provided a process for
preparing alumina and optionally other products, the process
comprising: leaching an aluminum-containing material with HCl so as
to obtain a leachate comprising aluminum ions and a solid, and
separating the solid from the leachate; reacting the leachate with
HCl so as to obtain a liquid and a precipitate comprising the
aluminum ions in the form of AlCl.sub.3, and separating the
precipitate from the liquid; heating the precipitate under
conditions effective for converting AlCl.sub.3 into Al.sub.2O.sub.3
and recovering gaseous HCl so-produced; and recycling the gaseous
HCl so-produced by contacting it with water so as to obtain a
composition having a concentration of about 18 to about 45 weight %
or about 25 to about 45 weight % and using the composition for
leaching the aluminum-containing material.
According to another aspect, there is provided a process for
preparing alumina and optionally other products, the process
comprising: leaching an aluminum-containing material with HCl so as
to obtain a leachate comprising aluminum ions and a solid, and
separating the solid from the leachate; reacting the leachate with
HCl so as to obtain a liquid and a precipitate comprising the
aluminum ions in the form of AlCl.sub.3, and separating the
precipitate from the liquid; heating the precipitate under
conditions effective for converting AlCl.sub.3 into Al.sub.2O.sub.3
and recovering gaseous HCl so-produced; and recycling the gaseous
HCl so-produced by contacting it with the leachate so as to
precipitate the aluminum ions in the form of
AlCl.sub.3.6H.sub.2O.
According to another aspect, there is provided a process for
preparing alumina and optionally other products, the process
comprising: leaching an aluminum-containing material with HCl so as
to obtain a leachate comprising aluminum ions and a solid, and
separating the solid from the leachate; reacting the leachate with
HCl so as to obtain a liquid and a precipitate comprising the
aluminum ions in the form of AlCl.sub.3, and separating the
precipitate from the liquid; and heating the precipitate under
conditions effective for converting AlCl.sub.3 into
Al.sub.2O.sub.3.
According to another aspect, there is provided a process for
preparing alumina and optionally other products, the process
comprising: leaching an aluminum-containing material with HCl so as
to obtain a leachate comprising aluminum ions and a solid, and
separating the solid from the leachate; reacting the leachate with
HCl so as to obtain a liquid and a precipitate comprising the
aluminum ions in the form of AlCl.sub.3, and separating the
precipitate from the liquid; and heating the precipitate under
conditions effective for converting AlCl.sub.3 into Al.sub.2O.sub.3
and optionally recovering gaseous HCl so-produced.
According to one aspect, there is provided a process for preparing
aluminum and optionally other products, the process comprising:
leaching an aluminum-containing material with HCl so as to obtain a
leachate comprising aluminum ions and a solid, and separating the
solid from the leachate; reacting the leachate with HCl so as to
obtain a liquid and a precipitate comprising the aluminum ions in
the form of AlCl.sub.3, and separating the precipitate from the
liquid; heating the precipitate under conditions effective for
converting AlCl.sub.3 into Al.sub.2O.sub.3; and converting
Al.sub.2O.sub.3 into aluminum.
According to another aspect, there is provided a process for
preparing aluminum and optionally other products, the process
comprising: leaching an aluminum-containing material with HCl so as
to obtain a leachate comprising aluminum ions and a solid, and
separating the solid from the leachate; reacting the leachate with
HCl so as to obtain a liquid and a precipitate comprising the
aluminum ions in the form of AlCl.sub.3, and separating the
precipitate from the liquid; heating the precipitate under
conditions effective for converting AlCl.sub.3 into Al.sub.2O.sub.3
and optionally recovering gaseous HCl so-produced; and converting
Al.sub.2O.sub.3 into aluminum.
According to another aspect, there is provided a process for
preparing various products, the process comprising: leaching an
aluminum-containing material comprising a first metal with HCl so
as to obtain a leachate comprising ions of the first metal and a
solid, and separating the solid from the leachate; reacting the
leachate with HCl so as to obtain a liquid and a precipitate
comprising a chloride of the first metal, and separating the
precipitate from the liquid; and heating the precipitate under
conditions effective for converting the chloride of the first metal
into an oxide of the first metal.
According to another aspect, there is provided a process for
preparing various products, the process comprising: leaching an
aluminum-containing material comprising a first metal with an acid
so as to obtain a leachate comprising ions of the first metal and a
solid, and separating the solid from the leachate; substantially
selectively removing ions of the first metal from the leachate,
thereby obtaining a composition; and substantially selectively
removing ions of a second metal from the composition.
According to another aspect, there is a process for treating an
aluminum-containing material comprising: leaching fly ash with an
acid so as to obtain a leachate and a solid residue, and separating
the leachate from the solid residue; at least partially removing
iron ions from the leachate by substantially selectively
precipitating the iron ions at a pH greater than 10 by reacting the
leachate with a base and at least partially removing the
precipitated iron ions from the leachate, thereby obtaining an
Al-rich composition comprising Al.sup.3+ ions; optionally purifying
the Al.sup.3+ ions; and converting the Al.sup.3+ ions into
alumina.
According to another aspect, there is a process for treating an
aluminum-containing material comprising: leaching the
aluminum-containing material with an acid so as to obtain a
leachate and a solid residue, and separating the leachate from the
solid residue; at least partially removing iron ions from the
leachate by substantially selectively precipitating the iron ions
at a pH of about 3 to about 6 by reacting the leachate with a base
and at least partially removing the precipitated iron ions from the
leachate, thereby obtaining an Al-rich composition comprising
Al.sup.3+ ions; optionally purifying the Al.sup.3+ ions; and
converting the Al.sup.3+ ions into alumina.
BRIEF DESCRIPTION OF DRAWINGS
In the following drawings, which represent by way of example only,
various embodiments of the disclosure:
FIG. 1 shows a bloc diagram of an example of process for preparing
alumina and various other products according to the present
disclosure;
FIG. 2 is an extraction curve for Al and Fe in which the extraction
percentage is expressed as a function of a leaching time in a
process according to an example of the present application;
FIG. 3 shows a bloc diagram of another example of process for
preparing alumina and various other products according to the
present disclosure;
FIG. 4 is a schematic representation of an example of a process for
purifying/concentrating HCl according to the present
disclosure;
FIG. 5 is a schematic representation of an example of a process for
purifying/concentrating HCl according to the present
disclosure;
FIG. 6 shows another bloc diagram of an example of process for
preparing alumina and various other products according to the
present disclosure; and
FIG. 7 shows another bloc diagram of an example of process for
preparing alumina and various other products according to the
present disclosure.
DETAILED DESCRIPTION OF VARIOUS EMBODIMENTS
The following non-limiting examples further illustrate the
technology described in the present disclosure.
The aluminum-containing material can be for example chosen from
aluminum-containing ores (such as aluminosillicate minerals, clays,
argillite, nepheline, mudstone, beryl, cryolite, garnet, spinel,
bauxite, kaolin or mixtures thereof can be used). The
aluminum-containing material can also be a recycled industrial
aluminum-containing material such as slag, red mud or fly ash.
The expression "red mud" as used herein refers, for example, to an
industrial waste product generated during the production of
alumina. For example, such a waste product can comprise silica,
aluminum, iron, calcium, and optionally titanium. It can also
comprise an array of minor constituents such as Na, K, Cr, V, Ni,
Ba, Cu, Mn, Pb, and/or Zn etc. For example, red mud can comprises
about 15 to about 80% by weight of Fe.sub.2O.sub.3, about 1 to
about 35% by weight Al.sub.2O.sub.3, about 1 to about 65% by weight
of SiO.sub.2, about 1 to about 20% by weight of Na.sub.2O, about 1
to about 20% by weight of CaO, and from 0 to about 35% by weight of
TiO.sub.2. According to another example, red mud can comprise about
30 to about 65% by weight of Fe.sub.2O.sub.3, about 10 to about 20%
by weight Al.sub.2O.sub.3, about 3 to about 50% by weight of
SiO.sub.2, about 2 to about 10% by weight of Na.sub.2O, about 2 to
about 8% by weight of CaO, and from 0 to about 25% by weight of
TiO.sub.2.
The expression "fly ashes" or "fly ash" as used herein refers, for
example, to an industrial waste product generated in combustion.
For example, such a waste product can contain various elements such
as silica, oxygen, aluminum, iron, calcium. For example, fly ash
can comprise silicon dioxide (SiO.sub.2) and aluminium oxide
(Al.sub.2O.sub.3). For example, fly ash can further comprises
calcium oxide (CaO) and/or iron oxide (Fe.sub.2O.sub.3). For
example fly ash can comprise fine particles that rise with flue
gases. For example, fly ash can be produced during combustion of
coal. For example, fly ash can also comprise at least one element
chosen from arsenic, beryllium, boron, cadmium, chromium, chromium
VI, cobalt, lead, manganese, mercury, molybdenum, selenium,
strontium, thallium, and/or vanadium. For example, fly ash can also
comprise rare earth elements and rare metals. For example, fly ash
can be considered as an aluminum-containing material. For example,
fly ash can comprise about 40 to about 50% by weight SiO.sub.2,
about 20 to about 30% by weight Al.sub.2O.sub.3, about 15 about 25%
by weight Fe.sub.2O.sub.3, about 1 to about 6% by weight Ca.sub.2O,
about 0 to about 2% by weight MgO, about 0 to about 2% Na.sub.2O
and about 1 to about 4% K.sub.2O
The expression "rare earth element" (also described as "REE") as
used herein refers, for example, to a rare element chosen from
scandium, yttrium, lanthanum, cerium, praseodymium, neodymium,
promethium, samarium, europium, gadolinium, terbium, dysprosium,
holmium, erbium, thulium, ytterbium, and lutetium. The expression
"rare metals" as used herein refers, for example, to rare metals
chosen from indium, zirconium, lithium, and gallium. These rare
earth elements and rare metals can be in various form such as the
elemental form (or metallic form), under the form of chlorides,
oxides, hydroxides etc. The expression "rare earths" as used in the
present disclosure as a synonym of "rare earth elements and rare
metals" that is described above.
The expression "at least one iron chloride" as used herein refers
to FeCl.sub.2, FeCl.sub.3 or a mixture thereof.
The term "hematite" as used herein refers, for example, to a
compound comprising .alpha.-Fe.sub.2O.sub.3.
The expression "iron ions" as used herein refers, for example to
ions comprising to at least one type of iron ion chosen from all
possible forms of Fe ions. For example, the at least one type of
iron ion can be Fe.sup.2+, Fe.sup.3+, or a mixture thereof.
The expression "aluminum ions" as used herein refers, for example
to ions comprising to at least one type of aluminum ion chosen from
all possible forms of Al ions. For example, the at least one type
of aluminum ion can be Al.sup.3+.
The expression "at least one aluminum ion", as used herein refers,
for example, to at least one type of aluminum ion chosen from all
possible forms of Al ions. For example, the at least one aluminum
ion can be Al.sup.3+.
The expression "at least one iron ion", as used herein refers, for
example, to at least one type of iron ion chosen from all possible
forms of Fe ions. For example, the at least one iron ion can be
Fe.sup.2+, Fe.sup.3+, or a mixture thereof.
The expression "at least one precipitated iron ion", as used herein
refers, for example, to at least one type of iron ion chosen from
all possible forms of Fe ions that was precipitated in a solid
form. For example, the at least one iron ion present in such a
precipitate can be Fe.sup.2+, Fe.sup.3+, or a mixture thereof.
Terms of degree such as "about" and "approximately" as used herein
mean a reasonable amount of deviation of the modified term such
that the end result is not significantly changed. These terms of
degree should be construed as including a deviation of at least
.+-.5% or at least .+-.10% of the modified term if this deviation
would not negate the meaning of the word it modifies.
For example, the material can be leached with HCl having a
concentration of about 10 to about 50 weight %, about 15 to about
45 weight %, of about 18 to about 45 weight % of about 18 to about
32 weight %, of about 20 to about 45 weight %, of about 25 to about
45 weight %, of about 26 to about 42 weight %, of about 28 to about
40 weight %, of about 30 to about 38 weight %, or between 25 and 36
weight %. For example, HCl at about 18 wt % or about 32 wt % can be
used.
Leaching can also be carried out by adding dry highly concentrated
acid (for example, 85%, 90% or 95%) in gas phase into the aqueous
solution. Alternatively, leaching can also be carried out by using
a weak acid solution (for example <3 wt %).
For example, leaching can be carried out by using HCl having a
concentration of about 18 to about 32 wt % in a first reactor and
then, by using HCl having concentration of about 90 to about 95%
(gaseous) in a second reactor.
For example, leaching can be carried out by using HCl having a
concentration of about 18 to about 32 wt % in a first reactor then,
by using HCl having concentration of about 90 to about 95%
(gaseous) in a second reactor; and by using HCl having
concentration of about 90 to about 95% (gaseous) in a third
reactor.
For example, leaching can be carried out under an inert gas
atmosphere (for example argon or nitrogen).
For example, leaching can be carried out under an atmosphere of
NH.sub.3.
For example, the material can be leached at a temperature of about
125 to about 225.degree. C., about 150 to about 200.degree. C.,
about 160 to about 190.degree. C., about 185 to about 190.degree.
C., about 160 to about 180.degree. C., about 160 to about
175.degree. C., or about 165 to about 170.degree. C.
For example, the material can be leached at a pressure of about 4
to about 10 barg, about 4 to about 8 barg, or about 5 to about 6
barg.
The leaching can be carried out under pressure (for example greater
than atmospheric pressure) into an autoclave. For example, it can
be carried out at a pressure of about 5 KPa to about 850 KPa, about
50 KPa to about 800 KPa, about 100 KPa to about 750 KPa, about 150
KPa to about 700 KPa, about 200 KPa to about 600 KPa, or about 250
KPa to about 500 KPa. The leaching can be carried out at a
temperature of at least 80.degree. C., at least 90.degree. C., or
about 100.degree. C. to about 110.degree. C. In certain cases, it
can be done at higher temperatures.
The leaching can also be carried out under pressure. For example,
the pressure can be about 100 to about 300 or about 150 to about
200 psig. The leaching can be carried out for about 30 minutes to
about 5 hours. It can be carried out at a temperature of about
60.degree. C. to about 200.degree. C.
For example, the processes can further comprise recycling the
gaseous HCl so-produced by contacting it with water so as to obtain
a composition having a concentration of about 18 to about 45 weight
% or 25 to about 45 weight %.
For example, the processes can further comprise recycling the
gaseous HCl so-produced by contacting it with water so as to obtain
a composition having a concentration of about 18 to about 45 weight
%, about 26 to about 42 weight %, about 28 to about 40 weight %,
about 30 to about 38 weight %, between 18 and 36 weight %, between
19 and 36 weight %, between 25 and 36 weight % or about 25 to about
45 weight % and optionally using the composition for leaching the
material.
For example, the liquid can comprise iron chloride. Iron chloride
can comprise at least one of FeCl.sub.2, FeCl.sub.3, and a mixture
thereof.
For example, the liquid can have an iron chloride concentration of
at least 30% by weight; and can then be hydrolyzed at a temperature
of about 155 to about 350.degree. C.
For example, the liquid can be concentrated to a concentrated
liquid having an iron chloride concentration of at least 30% by
weight; and then the iron chloride can be hydrolyzed at a
temperature of about 155 to about 350.degree. C. while maintaining
a ferric chloride concentration at a level of at least 65% by
weight, to generate a composition comprising a liquid and
precipitated hematite, and recovering the hematite.
For example, non-hydrolysable elements with hematite can be
concentrated back to a concentration of about 0.125 to about 52%
wt. in circulation loop in view of selective extraction.
For example, the liquid can be concentrated to a concentrated
liquid having a concentration of the at least one iron chloride of
at least 30% by weight; and then hydrolyzed at a temperature of
about 155 to about 350.degree. C.
For example, the liquid can be concentrated to a concentrated
liquid having a concentration of the at least one iron chloride of
at least 30% by weight; and then the at least one iron chloride is
hydrolyzed at a temperature of about 155 to about 350.degree. C.
while maintaining a ferric chloride concentration at a level of at
least 65% by weight, to generate a composition comprising a liquid
and precipitated hematite, and recovering the hematite.
For example, the liquid can be concentrated to a concentrated
liquid having a concentration of the at least one iron chloride of
at least 30% by weight; and then the at least one iron chloride is
hydrolyzed at a temperature of about 155 to about 350.degree. C.
while maintaining a ferric chloride concentration at a level of at
least 65% by weight, to generate a composition comprising a liquid
and precipitated hematite; recovering the hematite; and recovering
rare earth elements and/or rare metals from the liquid.
For example, the at least one iron chloride can be hydrolyzed at a
temperature of about, 150 to about 175, 155 to about 170 or 165 to
about 170.degree. C.
For example, the liquid can be concentrated to a concentrated
liquid having an iron chloride concentration of at least 30% by
weight; and then the iron chloride can be hydrolyzed at a
temperature of about 155 to about 350.degree. C. while maintaining
a ferric chloride concentration at a level of at least 65% by
weight, to generate a composition comprising a liquid and
precipitated hematite; recovering the hematite; and recovering rare
earth elements and/or rare metals from the liquid.
For example, the processes can further comprise, after recovery of
the rare earth elements and/or rare metals, reacting the liquid
with HCl so as to cause precipitation of MgCl.sub.2, and recovering
same.
For example, the processes can further comprise calcining
MgCl.sub.2 into MgO and optionally recycling HCl so-produced.
For example, the processes can further comprises, after recovery of
the rare earth elements and/or rare metals, reacting the liquid
with HCl, and substantially selectively precipitating
Na.sub.2SO.sub.4. For example, Na.sub.2SO.sub.4 can be precipitated
by reacting the liquid with H.sub.2SO.sub.4.
For example, the processes can further comprises, after recovery of
the rare earth elements and/or rare metals, reacting the liquid
with HCl, and substantially selectively precipitating
K.sub.2SO.sub.4. For example, K.sub.2SO.sub.4 can be precipitated
by adding H.sub.2SO.sub.4.
For example, the liquid can be concentrated to a concentrated
liquid having an iron chloride concentration of at least 30% by
weight; and then the iron chloride can be hydrolyzed at a
temperature of about 155 to about 350.degree. C. while maintaining
a ferric chloride concentration at a level of at least 65% by
weight, to generate a composition comprising a liquid and
precipitated hematite; recovering the hematite; and reacting the
liquid with HCl. For example, such processes can further comprises
reacting the liquid with H.sub.2SO.sub.4 so as to substantially
selectively precipitate Na.sub.2SO.sub.4. The processes can also
comprise further reacting the liquid with H.sub.2SO.sub.4 so as to
substantially selectively precipitating K.sub.2SO.sub.4.
For example, the processes can comprise reacting dry individual
salts (for example Na or K salts) obtained during the processes
with H.sub.2SO.sub.4 and recovering HCl while producing marketable
K.sub.2SO.sub.4 and Na.sub.2SO.sub.4 and recovering hydrochloric
acid of about 15 to about 90% wt.
For example, sodium chloride produced in the processes can undergo
a chemical reaction with sulfuric acid so as to obtain sodium
sulfate and regenerate hydrochloric acid. Potassium chloride can
undergo a chemical reaction with sulfuric acid so as to obtain
potassium sulfate and regenerate hydrochloric acid. Sodium and
potassium chloride brine solution can alternatively be the feed
material to adapted small chlor-alkali electrolysis cells. In this
latter case, common bases (NaOH and KOH) and bleach (NaOCl and
KOCl) are produced.
For example, the processes can further comprise, after recovery of
the rare earth elements and/or rare metals, recovering NaCl from
the liquid, reacting the NaCl with H.sub.2SO.sub.4, and
substantially selectively precipitating Na.sub.2SO.sub.4.
For example, the processes can further comprise, downstream of
recovery of the rare earth elements and/or rare metals, recovering
KCl from the liquid, reacting the KCl with H.sub.2SO.sub.4, and
substantially selectively precipitating K.sub.2SO.sub.4.
For example, the processes can further comprise, downstream of
recovery of the rare earth elements and/or rare metals, recovering
NaCl from the liquid, carrying out an electrolysis to generate NaOH
and NaOCl.
For example, the processes can further comprise, downstream of
recovery of the rare earth elements and/or rare metals, recovering
KCl from the liquid, reacting the KCl, carrying out an electrolysis
to generate KOH and KOCl.
For example, the liquid can be concentrated to a concentrated
liquid having a concentration of the at least one iron chloride of
at least 30% by weight; and then the at least one iron chloride is
hydrolyzed at a temperature of about 155 to about 350.degree. C.
while maintaining a ferric chloride concentration at a level of at
least 65% by weight, to generate a composition comprising a liquid
and precipitated hematite; recovering the hematite; and extracting
NaCl and/or KCl from the liquid.
For example, the processes can further comprise reacting the NaCl
with H.sub.2SO.sub.4 so as to substantially selectively precipitate
Na.sub.2SO.sub.4.
For example, the processes can further comprise reacting the KCl
with H.sub.2SO.sub.4 so as to substantially selectively precipitate
K.sub.2SO.sub.4.
For example, the processes can further comprise carrying out an
electrolysis of the NaCl to generate NaOH and NaOCl.
For example, the processes can further comprise carrying out an
electrolysis of the KCl to generate KOH and KOCl.
For example, the processes can comprise separating the solid from
the leachate and washing the solid so as to obtain silica having a
purity of at least 95%, at least 96%, at least 97%, at least 98%,
at least 99%, at least 99.5% or at least 99.9%.
For example, AlCl.sub.3 can be in the form of
AlCl.sub.3.6H.sub.2O.
For example, the processes can comprise reacting the leachate with
gaseous HCl so as to obtain the liquid and the precipitate
comprising the aluminum ions in the form of
AlCl.sub.3.6H.sub.2O.
For example, the processes can comprise reacting the leachate with
dry gaseous HCl so as to obtain the liquid and the precipitate
comprising the aluminum ions in the form of
AlCl.sub.3.6H.sub.2O.
For example, the processes can comprise reacting the leachate with
acid of at least 30% wt. that was recovered, regenerated and/or
purified as indicated in the present disclosure so as to obtain the
liquid and the precipitate comprising the aluminum ions in the form
of AlCl.sub.3.6H.sub.2O.
For example, the processes can comprise reacting the leachate with
gaseous HCl so as to obtain the liquid and the precipitate
comprising the aluminum ions, the precipitate being formed by
crystallization of AlCl.sub.3.6H.sub.2O.
For example, the processes can comprise reacting the leachate with
dry gaseous HCl so as to obtain the liquid and the precipitate
comprising the aluminum ions, the precipitate being formed by
crystallization of AlCl.sub.3.6H.sub.2O.
For example, aluminum ions can be precipitated under the form of
AlCl.sub.3 (for example AlCl.sub.3.6H.sub.2O) in a crystallizer,
for example, by adding HCl having a concentration of about 26 to
about 32 wt % or about 24 to about 26% wt.
For example, the gaseous HCl can have a HCl concentration of at
least 85% wt. or at least 90% wt.
For example, the gaseous HCl can have a HCl concentration of about
90% wt. or about 90% to about 95% wt.
For example, during the crystallization of AlCl.sub.3.6H.sub.2O,
the liquid can be maintained at a concentration of HCl of about 25
to about 35% by weight, about 30 to about 32% by weight or about 23
to about 26% by weight.
For example, the crystallization can be carried out at a
temperature of about 45 to about 65.degree. C. or about 50 to about
60.degree. C.
For example, the HCl can be obtained from the gaseous HCl
so-produced.
For example, in the processes of the present disclosure, a given
batch or quantity of the aluminum-containing material will be
leached, will then be converted into AlCl.sub.3.6H.sub.2O and when
the HCl generated during calcination of AlCl.sub.3.6H.sub.2O into
Al.sub.2O.sub.3 will be used for example to leach another given
batch or quantity of the aluminum-containing material.
For example, the processes can comprise heating the precipitate at
a temperature of at least 850, 900, 925, 930, 1000, 1100, 1200 or
1250.degree. C. for converting AlCl.sub.3.6H.sub.2O into
Al.sub.2O.sub.3.
For example, converting AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3
can comprise calcination of AlCl.sub.3.
For example, calcination is effective for converting
AlCl.sub.3.6H.sub.2O into beta-Al.sub.2O.sub.3.
For example, calcination is effective for converting
AlCl.sub.3.6H.sub.2O into alpha-Al.sub.2O.sub.3.
For example, converting AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3
can comprise carrying out a calcination via a two-stage circulating
fluid bed reactor or via a single stage circulating fluid bed, or
via any arrangement fluid bed, kiln, or a plasma system.
For example, converting AlCl.sub.3 into Al.sub.2O.sub.3 can
comprise carrying out a calcination via a two-stage circulating
fluid bed reactor that comprises a preheating system.
For example, converting AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3
can comprise carrying out a calcination at low temperature, for
example, of at least about 350.degree. C., at least 375.degree. C.
about 300 to about 600.degree. C., about 325 to about 550.degree.
C., about 350 to about 500.degree. C., about 375 to about
450.degree. C., about 375 to about 425.degree. C., or about 385 to
about 400.degree. C. and/or injecting steam.
For example, converting AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3
can comprise carrying out a calcination at low temperature, for
example, at least 350.degree. C. and/or injecting steam.
For example, converting AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3
can comprise carrying out a calcination at low temperature, for
example, less than 600.degree. C. and/or injecting steam.
For example, converting AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3
can comprise carrying out a calcination by using coal as combustion
source and by using a degasification unit.
For example, steam (or water vapor) can be injected at a pressure
of about 200 to about 700 psig, about 300 to about 700 psig, about
400 to about 700 psig, about 550 to about 650 psig, about 575 to
about 625 psig, or about 590 to about 610 psig.
For example, steam (or water vapor) can be injected and a plasma
torch can be used for carrying fluidization.
For example, the steam (or water vapor) can be overheated.
For example, the steam (or water vapor) can be at a temperature of
about 300 to about 400.degree. C.
For example, acid from the offgases generated during calcination
can be then treated via a gas phase purification process.
For example, converting AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3
can comprise carrying out a calcination by means of carbon monoxide
(CO).
For example, converting AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3
can comprise carrying out a calcination by means of a Refinery Fuel
Gas (RFG).
For example, calcination can be carried out by injecting water
vapor or steam and/or by using a combustion source chosen from
fossil fuels, carbon monoxide, a Refinery Fuel Gas, coal, or
chlorinated gases and/or solvents.
For example, the processes can comprise converting
AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3 by carrying out a
calcination of AlCl.sub.3.6H.sub.2O that is provided by the
combustion of gas mixture that is a an incoming smelter gas or a
reducer offgas.
For example, the processes can comprise converting
AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3 by carrying out a
calcination of AlCl.sub.3.6H.sub.2O that is provided by the
combustion of gas mixture that is a an incoming smelter gas or a
reducer offgas.
For example, the processes can comprise converting
AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3 by carrying out a
calcination of AlCl.sub.3.6H.sub.2O that is provided by the
combustion of gas mixture that comprises:
CH.sub.4: 0 to about 1% vol;
C.sub.2H.sub.6: 0 to about 2% vol;
C.sub.3H.sub.8: 0 to about 2% vol;
C.sub.4H.sub.10: 0 to about 1% vol;
N.sub.2: 0 to about 0.5% vol;
H.sub.2: about 0.25 to about 15.1% vol;
CO: about 70 to about 82.5% vol; and
CO.sub.2: about 1.0 to about 3.5% vol.
For example, O.sub.2 can be substantially absent from the
mixture.
For example, calcination can be carried out by injecting water
vapor or steam and/or by using a combustion source chosen from
natural gas or propane.
For example, calcination can be carried out by providing heat by
means of electric heating, gas heating, microwave heating and
plasma heating.
The obtained alumina can be washed by demineralized water so as to
at least partially remove NaCl and/or KCl.
For example, the fluid bed reactor can comprise a metal catalyst
chosen from metal chlorides.
For example, the fluid bed reactor can comprise a metal catalyst
that is FeCl.sub.3, FeCl.sub.2 or a mixture thereof.
For example, the fluid bed reactor can comprise a metal catalyst
that is FeCl.sub.3.
For example, the preheating system can comprise a plasma torch.
For example, steam can be used as the fluidization medium heating.
Heating can also be electrical.
For example, a plasma torch can be used for preheating the
calcination reactor.
For example, a plasma torch can be used for preheating air entering
in the calcination reactor.
For example, a plasma torch can be used for preheating a fluid
bed.
For example, the plasma torch can be effective for generating steam
that is injected into a calcination reactor.
For example, the plasma torch can be effective for generating steam
that is as fluidization medium in a fluid bed reactor.
For example, the calcination medium can be substantially neutral in
terms of O.sub.2 (or oxidation). For example, the calcination
medium can favorize reduction (for example a concentration of CO of
about 100 ppm).
For example, the calcination medium is effective for preventing
formation of Cl.sub.2.
For example, the processes can comprise converting
AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3 by carrying out a
calcination of AlCl.sub.3.6H.sub.2O that is provided by the
combustion of gas mixture that comprises:
CH.sub.4: 0 to about 1% vol;
C.sub.2H.sub.6: 0 to about 2% vol;
C.sub.3H.sub.8: 0 to about 2% vol;
C.sub.4H.sub.10: 0 to about 1% vol;
N.sub.2: 0 to about 0.5% vol;
H.sub.2: about 0.25 to about 15.1% vol;
CO: about 70 to about 82.5% vol; and
CO.sub.2: about 1.0 to about 3.5% vol.
Such a mixture can be efficient for reduction in off gas volume of
15.3 to 16.3%; therefore the capacity increases of 15.3 to 16.3%
proven on practical operation of the circulating fluid bed. Thus
for a same flow it represents an Opex of 0.65*16.3%=10.6%.
For example, the air to natural gas ratio of (Nm.sup.3/h over
Nm.sup.3/h) in the fluid bed can be about 9.5 to about 10
For example, the air to CO gas ratio of (Nm.sup.3/h over
Nm.sup.3/h) in the fluid bed can be about 2 to about 3.
For example, the processes can comprise, before leaching the
aluminum-containing material, a pre-leaching removal of fluorine
optionally contained in the aluminum-containing material.
For example, the processes can comprise leaching of the
aluminum-containing material with HCl so as to obtain the leachate
comprising aluminum ions and the solid, separating the solid from
the leachate; and further treating the solid so as to separate
SiO.sub.2 from TiO.sub.2 that are contained therein.
For example, the processes can comprise leaching the
aluminum-containing material with HCl so as to obtain the leachate
comprising aluminum ions and the solid, separating the solid from
the leachate; and further treating the solid with HCl so as to
separate Si from Ti that are contained therein.
For example, the processes can comprise leaching the
aluminum-containing material with HCl so as to obtain the leachate
comprising aluminum ions and the solid, separating the solid from
the leachate; and further treating the solid with HCl at a
concentration of less than 20% wt., at a temperature of less than
85.degree. C., in the presence of MgCl.sub.2, so as to separate Si
from Ti that are contained therein.
For example, the processes can comprise leaching said fly ash with
HCl so as to obtain the leachate comprising aluminum ions and the
solid, separating the solid from the leachate; and further treating
the solid so as to separate SiO.sub.2 from TiO.sub.2 that are
contained therein.
For example, the processes can comprise comprising leaching the fly
ash with HCl so as to obtain the leachate comprising aluminum ions
and the solid, separating the solid from the leachate; and further
treating the solid with HCl so as to separate SiO.sub.2 from
TiO.sub.2 that are contained therein.
For example, the processes can comprise leaching the fly ash with
HCl so as to obtain the leachate comprising aluminum ions and the
solid, separating the solid from the leachate; and further treating
the solid with HCl at a concentration of less than 20% by weight,
at a temperature of less than 85.degree. C., in the presence of
MgCl, so as to separate SiO.sub.2 from TiO.sub.2 that are contained
therein.
For example, converting AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3
can comprise carrying out a one-step calcination.
For example, the processes can comprise converting
AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3 by carrying out a
calcination of AlCl.sub.3.6H.sub.2O, the calcination comprising
steam injection.
For example, calcination can be carried out at different
temperatures with steam. Temperature applied of superheated steam
can be of about 350.degree. C. to about 550.degree. C. or about
350.degree. C. to about 940.degree. C. or about 350.degree. C. to
about 1200.degree. C.
For example, multi stage evaporation step of the hydrolyser can be
carried out to reduce drastically energy consumption.
For example, the processes can be effective for providing an
Al.sub.2O.sub.3 recovery yield of at least 93%, at least 94%, at
least 95%, about 90 to about 95%, about 92 to about 95%, or about
93 to about 95%.
For example, the processes can be effective for providing a
Fe.sub.2O.sub.3 recovery yield of at least 98%, at least 99%, about
98 to about 99.5%, or about 98.5 to about 99.5%.
For example, the processes can be effective for providing a MgO
recovery yield of at least 96%, at least 97%, at least 98%, or
about 96 to about 98%.
For example, the processes can be effective for providing a HCl
recovery yield of at least 98%, at least 99%, about 98 to about
99.9% or about 98 to about 99.99%.
For example, the processes can be effective for providing chlorides
of rare earth elements (REE-Cl) and chlorides of rare metals
(RM-Cl) in recovery yields of about 75% to about 96.5% by using
internal processes via an internal concentration loop.
For example, the processes can be effective for providing
hydrochloric acid recovery yield of about 99.75% with
non-hydrolysable elements.
For example, the aluminum-containing material can be argillite.
For example, the aluminum-containing material can be bauxite.
For example, the aluminum-containing material can be red mud.
For example, the aluminum-containing material can be fly ash.
For example, the aluminum-containing material can be chosen from
industrial refractory materials.
For example, the aluminum-containing material chosen from
aluminosilicate minerals.
For example, the processes can be effective for avoiding producing
red mud.
For example, the alumina and the other products are substantially
free of red mud.
For example, HCl can be recycled. For example, such a recycled HCl
can be concentrated and/or purified.
For example, gaseous HCl can be concentrated and/or purified by
means of H.sub.2SO.sub.4. For example, gaseous HCl can be treated
with H.sub.2SO.sub.4 so as to reduce the amount of water present in
the gaseous HCl. For example, gaseous HCl can be passed through a
packed column where it is contacted with a H.sub.2SO.sub.4
countercurrent flow. For example, by doing so, concentration of HCl
can be increased by at least 50% wt., at least 60% wt., at least
70% wt., at least 75% wt., at least 80% wt., about 50% wt. to about
80% wt., about 55% wt. to about 75% wt., or about 60% wt. For
example, the column can be packed with a polymer such as
polypropylene (PP) or polytrimethylene terephthalate (PTT).
For example, gaseous HCl can be concentrated and/or purified by
means of CaCl.sub.2 or LiCl. For example, gaseous HCl can be passed
through a column packed with CaCl.sub.2 or LiCl.
For example, the concentration of gaseous HCl can be increased from
a value below the azeotropic point before treatment to a value
above the azeotropic point after treatment.
For example, the various products obtained by the processes of the
present disclosure such as alumina, hematite, titanium oxides,
magnesium oxides, rare earth elements and rare metals can be
further purified by means of a plasma torch. For example, the rare
earth elements and rare metals, once isolated, can be individually
injected into a plasma torch so as to further purify them.
For example, the acid can be chosen from HCl, HNO.sub.3,
H.sub.2SO.sub.4 and mixtures thereof.
For example, the first metal can be aluminum or iron. For example,
the second metal can be aluminum or iron.
For example, when the first metal is aluminum, the aluminum ions
can be removed from said leachate by reacting the leachate with an
acid (such as HCl) so as to obtain a liquid and a precipitate
comprising said aluminum ions (for example in the form of
AlCl.sub.3), and separating said precipitate from said liquid.
Then, iron ions can be recovered from the liquid by precipitation,
hydrolysis, purification etc.
For example, when the first metal is iron, the iron ions can be
removed from said leachate by leachate with a base (such as NaOH or
KOH) so as to obtain a liquid and a precipitate comprising said
iron ions, and separating said precipitate from said liquid. Then,
aluminum ions can be recovered from the liquid by precipitation,
hydrolysis, purification etc.
For example, the processes can comprise precipitating said
Al.sup.3+ ions under the form of Al(OH).sub.3. For example, wherein
precipitating said Al.sup.3+ under the form of Al(OH).sub.3 is
carried out at a pH of about 7 to about 10, about 9 to about 10,
about 9.2 to about 9.8, about 9.3 to about 9.7, about 9.5, about
7.5 to about 8.5, about 7.8 to about 8.2 or about 8.
For example, the iron ions can be precipitated at a pH greater than
11, a pH greater than 12, a pH comprised between 10 and 11, a pH of
about 11.5 to about 12.5 or of about 11.8 to about 12.0.
For example, the iron ions can be precipitated at a pH of about 3.0
to about 5.5, about 3 to about 5, about 3 to about 4, about 3.0 to
about 3.5, about 3.5 to about 4.0, about 4 to about 5, about 4.5 to
about 5.0, about 5 to about 6 by adding said base.
For example, when the first metal to be removed is iron, the
processes can be carried out in a manner similar as described in
WO2008/141423 or in WO2012/065253 and by using, for example, using
an aluminum-containing material as described in the present
disclosure as starting material. These document are hereby
integrated by reference in their entirety.
For example, the Al.sup.3+ ions can be purified.
For example, the processes can further comprise converting alumina
(Al.sub.2O.sub.3) into aluminum. Conversion of alumina into
aluminum can be carried out, for example, by using the Hall-Heroult
process. References is made to such a well known process in various
patents and patent applications such as US 20100065435; US
20020056650; U.S. Pat. Nos. 5,876,584; 6,565,733. Conversion can
also be carried out by means of other methods such as those
described in U.S. Pat. Nos. 7,867,373; 4,265,716; 6,565,733
(converting alumina into aluminum sulfide followed by the
conversion of aluminum sulfide into aluminum.). For example,
aluminium can be produced by using a reduction environment and
carbon at temperature below 200.degree. C. Aluminum can also be
produced by reduction using potassium and anhydrous aluminum
chloride Wohler Process).
For example, converting AlCl.sub.3 into Al.sub.2O.sub.3 can be done
under an inert gas atmosphere.
For example, converting AlCl.sub.3 into Al.sub.2O.sub.3 can be done
under a nitrogen atmosphere.
For examples, the processes of the present disclosure can be
continuous processes or semi-continuous processes.
According to one example as shown in FIG. 1, the processes can
involve the following steps (the reference numbers in FIG. 1
correspond to the following steps):
1--The aluminum-containing material is reduced to an average
particle size of about 50 to about 80 .mu.m.
2--The reduced and classified material is treated with hydrochloric
acid which allows for dissolving, under a predetermined temperature
and pressure, the aluminum with other elements like iron, magnesium
and other metals including rare earth elements and/or rare metals.
The silica and titanium (if present in raw material) remain totally
undissolved.
3--The mother liquor from the leaching step then undergoes a
separation, a cleaning stage in order to separate the purified
silica from the metal chloride in solution. The purified silica can
then optionally undergo one or two additional leaching stages (for
example at a temperature of about 150 to about 160.degree. C.) so
as to increase the purity of silica above 99.9%. TiO.sub.2
contained in silica can be separated from silica through a leach
made by using HCl and MgCl.sub.2 as a lixiviant composition.
4--The spent acid (leachate) obtained from step 1 is then brought
up in concentration with dry and highly concentrated gaseous
hydrogen chloride by sparging this one into a crystallizer. This
results into the crystallization of aluminum chloride hexahydrate
(precipitate) with a minimum of other impurities. Depending on the
concentration of iron chloride at this stage, further
crystallization step(s) can be required. The precipitate is then
separated from the liquid.
5--The aluminum chloride hexahydrate is then calcined (for example
by means of a rotary kiln, fluid bed, etc) at high temperature in
order to obtain the alumina form. Highly concentrated gaseous
hydrogen chloride is then recovered and excess is brought in
aqueous form to the highest concentration possible so as to be used
(recycled) in the acid leaching step. Acid can also be directly
sent in gas phase to the acid purification stage to increase HCl
concentration from about 30 wt % to about 95 wt %. This can be
done, for example, during drying stage.
6--Iron chloride (the liquid obtained from step 4) is then
pre-concentrated and hydrolyzed at low temperature in view of the
Fe.sub.2O.sub.3 (hematite form) extraction and acid recovery from
its hydrolysis. All heat recovery from the calcination step (step
5), the leaching part exothermic reaction (step 1) and other
section of the processes is being recovered into the
pre-concentrator.
10--After the removal of hematite, a solution rich in rare earth
elements and/or rare metals can be processed. As it can be seen in
FIG. 3, an internal recirculation can be done (after the removal of
hematite) and the solution rich in rare earth elements and/or rare
metals can be used for crystallization stage 4. Extraction of the
rare earth elements and/or rare metals can be done as described in
PCT/CA2012/000253 and/or PCT/CA2012000419. These two documents are
hereby integrated by reference in their entirety.
Other non-hydrolysable metal chlorides (Me--Cl) such as MgCl.sub.2
and others then undergo the following steps:
7--The solution rich in magnesium chloride and other
non-hydrolysable products at low temperature is then brought up in
concentration with dry and highly concentrated gaseous hydrogen
chloride by sparging it into a crystallizer. This results into the
precipitation of magnesium chloride as an hexahydrate, for example
after sodium and potassium chloride removal.
8--Magnesium chloride hexahydrate is then calcined (either through
a rotary kiln, fluid bed, etc.) and hydrochloric acid at very high
concentration is thus regenerated and brought back to the leaching
step.
9--Other Me--Cl undergo a standard pyrohydrolysis step where mixed
oxides (Me--O) can be produced and hydrochloric acid at the
azeotropic point (20.2% wt.) is regenerated.
NaCl can undergo chemical reaction with H.sub.2SO.sub.4 to produce
Na.sub.2SO.sub.4 and HCl at a concentration at or above azeotropic
concentration. Moreover, KCl can undergo chemical reaction with
H.sub.2SO.sub.4 to produce K.sub.2SO.sub.4 and HCl having a
concentration that is above the azeotropic concentration. Sodium
and potassium chloride brine solution can be the feed material to
adapted small chlor-alkali electrolysis cells. In this latter case,
common bases (NaOH and KOH) and bleach (NaOCl and KOCl) are
produced as well as HCl.
For example, the liquid can be concentrated to a concentrated
liquid having an iron chloride concentration of at least 30% by
weight; and then the iron chloride can be hydrolyzed at a
temperature of about 155 to about 350.degree. C. while maintaining
a ferric chloride concentration at a level of at least 65% by
weight, to generate a composition comprising a liquid and
precipitated hematite, and recovering the hematite.
For example, the liquid can be concentrated to a concentrated
liquid having an iron chloride concentration of at least 30% by
weight; and then the iron chloride can be hydrolyzed at a
temperature of about 155 to about 350.degree. C. while maintaining
a ferric chloride concentration at a level of at least 65% by
weight, to generate a composition comprising a liquid and
precipitated hematite; recovering the hematite; and recovering rare
earth elements and/or rare metals from the liquid. For example, the
processes can further comprise, after recovery of the rare earth
elements and/or rare metals, reacting the liquid with HCl so as to
cause precipitation of MgCl.sub.2, and recovering same.
However, the person skilled in the art will understand that the
continuous processes can handle high percentages of silica
(>55%) and impurities as well as relatively low percentages of
aluminum (for example as low as about 15%) and still being
economically and technically viable. Satisfactory yields can be
obtained (>93-95%) on Al.sub.2O.sub.3 and greater than 75%, 85
or 90% on rare earth elements and/or rare metals. No pre-thermal
treatment in most cases are required. The processes disclosed in
the present disclosure involve special techniques on leaching and
acid recovery at very high strength, thereby offering several
advantages over alkaline processes.
In step 1 the mineral, whether or not thermally treated is crushed,
milled, dried and classified to have an average particle size of
about 50 to about 80 .mu.m.
In step 2, the milled raw material is introduced into the reactor
and will undergo the leaching phase.
The leaching hydrochloric acid used in step 2 can be a recycled or
regenerated acid from steps 5, 6, 8, 9, 10 and 11 (see FIG. 3) its
concentration can vary from 15% to 45% weight percent. Higher
concentration can be obtained using membrane separation, cryogenic
and/or high pressure approach. The acid leaching can be carried out
under pressure and at temperature close to its boiling point thus,
allowing a minimal digestion time and extended reaction extent
(90%-100%). Leaching (step 2) can be accomplished in a
semi-continuous mode where spent acid with residual free
hydrochloric acid is replaced, following pressurization, by highly
concentrated acid at a certain stage of the reaction or allowing a
reduced acid/mineral ratio, thereby reducing reaction time and
improving reaction kinetics. For example, kinetic constant k can
be: 0.5-0.75 g/moleL, or 0.65-0.82 g/moleL.
As previously indicated, alkali metals, iron, magnesium, sodium,
calcium, potassium, rare earth elements and other elements will
also be in a chloride form at different stages. Silica and
optionally titanium can remain undissolved and will undergo (step
3) a liquid/solid separation and cleaning stage. The processes of
the present disclosure tend to recover maximum amount of free
hydrochloric acid left and chlorides in solution in order to
maximize hydrochloric acid recovery yield, using techniques such as
rake classifying, filtration with band filters, centrifugation, and
others. Pure SiO.sub.2 (one additional leaching stage) cleaning
with nano water purity 99% min. Mother liquor free of silica is
then named as spent acid (various metal chlorides and water) and
goes to the crystallization step (step 4).
In step 4, the spent acid (or leachate) with a substantial amount
of aluminum chloride is then saturated with dry and highly
concentrated gaseous hydrogen chloride obtained or recycled from
step 5 or with aqueous HCl>30% wt., which results in the
precipitate of aluminum chloride hexahydrate
(AlCl.sub.3.6H.sub.2O). The precipitate retained is then washed and
filtered or centrifuged before being fed to the calcination stage
(step 5). The remaining of the spent acid from step 4 is then
processed to acid recovery system (steps 6 to 8) where pure
secondary products will be obtained.
In step 5, aluminum oxide (alumina) is directly obtained from high
temperature conditions. The highly concentrated hydrogen chloride
in gaseous form obtained can be fed to steps 4 and 7 for
crystallization where it can be treated through hydrophobic
membranes. The excess hydrogen chloride is absorbed and used as
regenerated acid to the leaching step 2 as highly concentrated
acid, higher than the concentration at the azeotropic point
(>20.2%). For example, such a concentration can be about 18 to
about 45 weight %, about 25 to about 45 weight % or between 25 and
36 weight %. Acid can also be redirected in gas phase directly
(>30 wt %) to acid purification.
After step 4, various chlorides derivatives (mainly iron with
magnesium and rare earth elements and rare metals) are next
subjected to an iron extraction step. Such a step can be carried
out for example by using the technology disclosed in WO
2009/153321, which is hereby incorporated by reference in its
entirety. Moreover, hematite can be seeded for crystal growth. For
example, hematite seeding can comprise recirculating the
seeding.
In step 6, a hydrolysis at low temperature (155-350.degree. C.) is
carried out and pure Fe.sub.2O.sub.3 (hematite) is being produced
and hydrochloric acid of at least 15% concentration is being
regenerated. The method as described in WO 2009/153321 is
processing the solution of ferrous chloride and ferric chloride,
possible mixtures thereof, and free hydrochloric acid through a
series of steps pre-concentration step, oxidation step where
ferrous chloride is oxidized into ferric form, and finally through
an hydrolysis step into an operational unit called hydrolyser where
the ferric chloride concentration is maintained at 65 weight % to
generate a rich gas stream where concentration ensures a hydrogen
chloride concentration of 15-20.2% and a pure hematite that will
undergo a physical separation step. Latent heat of condensation is
recovered to the pre-concentration and used as the heating input
with excess heat from the calcination stage (step 5).
The mother liquor from the hydrolyser (step 6) can be recirculated
partially to first step crystallization process where an increase
in concentration of non-hydrolysable elements is observed. After
iron removal, the liquor is rich in other non-hydrolysable elements
and mainly comprises magnesium chloride or possible mixture of
other elements (various chlorides) and rare earth elements and rare
metals.
Rare earth elements and rare metals in form of chlorides are highly
concentrated in percentage into the hydrolyser operational unit
(step 6) and are extracted from the mother liquor (step 10) where
various known techniques can be employed to extract a series of
individual RE-O (rare earth oxides). Among others, the processes of
the present disclosure allows to concentrate to high concentration
the following elements, within the hydrolyser: scandium (Sc),
galium (Ga), yttrium (Y), dysperosium (Dy), cerium (Ce),
praseodynium (Pr), neodynium (Nd), europium (Eu), lanthanum (La),
samarium (Sm), gadolinium, (Gd), erbium (Er), zirconium (Zr) and
mixtures of thereof. Technologies that can be used for extracting
rare earth elements and/or rare metals can be found, for example,
in Zhou et al. in RARE METALS, Vol. 27, No. 3, 2008, p 223-227, and
in US 2004/0042945, hereby incorporated by reference in their
entirety. The person skilled in the art will also understand that
various other processes normally used for extracting rare earth
elements and/or rare metals from the Bayer process can also be
used. For example, various solvent extraction techniques can be
used. For certain elements, a technique involving octylphenyl acid
phosphate (OPAP) and toluene can be used. HCl can be used as a
stripping agent. This can be effective for recovering
Ce.sub.2O.sub.3, Sc.sub.2O.sub.3, Er.sub.2O.sub.3 etc. For example,
different sequence using oxalic acid and metallic iron for ferric
chloride separation can be used.
The spent acid liquor from steps 6 and 10 rich in value added
metals, mainly magnesium, is processed to step 7. The solution is
saturated with dry and highly concentrated gaseous hydrogen
chloride from step 5, which results in the precipitation of
magnesium chloride hexahydrate. For example, same can be
accomplished with HCl in aqueous form over 30% wt. The precipitate
retained, is fed to a calcination stage step 8 where pure MgO
(>98% wt.) is obtained and highly concentrated hydrochloric acid
(for example of at least 38%) is regenerated and diverted to the
leaching step (step 2). An alternative route for step 7 is using
dry gaseous hydrochloric acid from step 8.
In step 9, metal chlorides unconverted are processed to a
pyrohydrolysis step (700-900.degree. C.) to generate mixed oxides
and where hydrochloric acid from 15-20.2% wt. concentration can be
recovered.
According to another example as shown in FIG. 3, the processes can
be similar to the example shown in FIG. 1 but can comprise some
variants as below discussed.
In fact, as shown in FIG. 3, the processes can comprise (after step
6 or just before step 10) an internal recirculation back to the
crystallization step 4. In such a case. The mother liquor from the
hydrolyser (step 6) can be recirculated fully or partially to the
crystallization of step 4 where a concentration increase will occur
with respect to the non-hydrolysable elements including rare earth
elements and/or rare metals.
Such a step can be useful for significantly increasing the
concentration of rare earth elements and/or rare metals, thereby
facilitating their extraction in step 10.
With respect to step 7, the solution rich in magnesium chloride and
other non-hydrolysable products at low temperature is, as
previously discussed, then brought up in concentration with dry and
highly concentrated gaseous hydrogen chloride by sparging it into a
crystallizer. This can result into the precipitation of magnesium
chloride as an hexahydrate (for example after sodium and potassium
chloride removal). This can also be accomplished with HCl in
aqueous form.
As shown in FIG. 3, an extra step 11 can be added. Sodium chloride
can undergo a chemical reaction with sulfuric acid so as to obtain
sodium sulfate and regenerate hydrochloric acid at a concentration
at or above the azeotropic point. Potassium chloride can undergo a
chemical reaction with sulfuric acid so as to obtain potassium
sulfate and regenerate hydrochloric acid at a concentration above
the azeotropic concentration. Sodium and potassium chloride brine
solution can be the feed material to adapted small chlor-alkali
electrolysis cells. In this latter case, common bases (NaOH and
KOH) and bleach (NaOCl and KOCl) are produced and can be reused to
some extent in other areas of the processes of the present
disclosure (scrubber, etc.).
The following are non-limitative examples.
EXAMPLE 1
Preparation of Alumina and Various Other Products
As a starting material a sample of clay was obtained from the
Grande Vallee area in Quebec, Canada.
These results represent an average of 80 tests carried out from
samples of about 900 kg each.
Crude clay in the freshly mined state after grinding and
classification had the following composition: Al.sub.2O.sub.3:
15%-26%; SiO.sub.2: 45%-50%; Fe.sub.2O.sub.3: 8%-9%; MgO: 1%-2%;
Rare earth elements and/or rare metals: 0.04%-0.07%; LOI:
5%-10%.
This material is thereafter leached in a two-stage procedure at
140-170.degree. C. with 18-32 weight % HCl. The HCl solution was
used in a stoichiometric excess of 10-20% based on the
stoichiometric quantity required for the removal of the acid
leachable constituents of the clay. In the first leaching stage of
the semi-continuous operation (step 2), the clay was contacted for
2.5 hours with required amount or certain proportion of the total
amount of hydrochloric acid. After removal of the spent acid, the
clay was contacted again with a minimum 18 weight % hydrochloric
acid solution for about 1.5 hour at same temperature and
pressure.
A typical extraction curve obtained for both iron and aluminum for
a single stage leaching is shown in FIG. 2.
The leachate was filtered and the solid was washed with water and
analyzed using conventional analysis techniques (see step 3 of FIG.
1). Purity of obtained silica was of 95.4% and it was free of any
chlorides and of HCl.
In another example, the purity of the silica was 99.67% through an
extra leaching step.
After the leaching and silica removal, the concentration of the
various metal chlorides was: AlCl.sub.3: 15-20%; FeCl.sub.2: 4-6%;
FeCl.sub.3: 0.5-2.0%; MgCl.sub.2: 0.5-2.0%; REE-Cl: 0.1-2% Free
HCl: 5-50 g/l
Spent acid was then crystallized using about 90 to about 98% pure
dry hydrochloric acid in gas phase in two stages with less than 25
ppm iron in the aluminum chloride hexahydrate formed. The
concentration of HCl in solution (aqueous phase) was about 22 to
about 32% or 25 to about 32%, allowing 95.3% of Al.sub.2O.sub.3
recovery. The recovered crystallized material (hydrate form of
AlCl.sub.3 having a minimum purity of 99.8%) was then calcined at
930.degree. C. or 1250.degree. C., thus obtaining the .alpha. form
of the alumina. Heating at 930.degree. C. allows for obtaining the
beta-form of alumina while heating at 1250.degree. C. allows for
obtaining the alpha-form.
Another example was carried out at low temperature (decomposition
and calcination at about 350.degree. C.) and the .alpha. form of
the alumina was less than 2%.
HCl concentration in gas phase exiting the calcination stage was
having a concentration greater than 30% and was used (recycled) for
crystallization of the AlCl.sub.3 and MgCl.sub.2. Excess of
hydrochloric acid is absorbed at the required and targeted
concentration for the leaching steps.
Iron chloride (about 90 to about 99.5%% in ferric form) is then
sent to a hydrothermal process in view of its extraction as pure
hematite (Fe.sub.2O.sub.3). This can be done by using the
technology described in WO 2009/153321 of low temperature
hydrolysis with full heat recovery from calcining, pyrohydrolysis
and leaching stage.
Rare earth elements and rare metals are extracted from the mother
liquor of the hydrolyzer where silica, aluminum, iron and a great
portion of water have been removed and following preconcentration
from hydrolyser to crystallization. It was measured that rare earth
elements can be concentrated by a factor of about 4.0 to 10.0 on
average within the hydrolyzer itself on a single pass through it
i.e. without concentration loop. The following concentration
factors have been noted within the hydrolyzer (single pass):
Ce>6
La>9
Nd>7
Y>9
Remaining magnesium chloride is sparged with dry and highly
concentrated hydrochloric acid and then calcinated to MgO while
recovering high concentration acid (for example up to 38.4%).
Mixed oxides (Me--O) containing other non-hydrolysable components
were then undergoing a pyrohydrolysis reaction at 700-800.degree.
C. and recovered acid (15-20.2% wt.) was rerouted for example to
the leaching system.
Overall Yields Obtained:
Al.sub.2O.sub.3: 93.0-95.03% recovery; Fe.sub.2O.sub.3: 92.65-99.5%
recovery; Rare earth elements: 95% minimum recovery (mixture); MgO:
92.64-98.00% recovery; Material discarded: 0-5% maximum; HCl global
recovery: 99.75% minimum; HCl strength as feed to leaching 15-32%
(aqueous); 95% (gas) Red mud production: none.
EXAMPLE 2
Preparation of Alumina and Various Other Products
A similar feed material (bauxite instead of clay) was processed as
per in example 1 up to the leaching stage and revealed to be easily
leachable under the conditions established in example 1. It
provided an extraction percentage of 100% for the iron and over
90-95% for aluminum. The technology was found to be economically
viable and no harmful by-products (red mud) were generated. Samples
tested had various concentrations of Al.sub.2O.sub.3 (up to 51%),
Fe.sub.2O.sub.3 (up to 27%) and MgO (up to 1.5%). Gallium
extraction of 97.0% was measured. Scandium extraction was 95%.
EXAMPLE 3
HCl Gas Enrichment and Purification: H.sub.2SO.sub.4 Route
H.sub.2SO.sub.4 can be used for carrying out purification of HCl.
It can be carried out by using a packing column with
H.sub.2SO.sub.4 flowing counter currently (see FIG. 4). This allows
for converting the recovered HCl into HCl having a concentration
above the azeotropic point (20.1% wt) and increase its
concentration by about 60 to about 70% at minimum.
Water is absorbed by H.sub.2SO.sub.4 and then H.sub.2SO.sub.4
regeneration is applied where H.sub.2SO.sub.4 is brought back to a
concentration of about 95 to about 98% wt. Water release at this
stage free of sulphur is recycled back and used for crystallization
dissolution, etc. Packing of the column can comprise polypropylene
or polytrimethylene terephthalate (PTT).
Combustion energy can be performed with off gas preheating air and
oxygen enrichment. Oxygen enrichment: +2% represents flame
temperature increase by: 400.degree. C. maximum.
EXAMPLE 4
HCl Gas Enrichment and Purification: Calcium Chloride to Calcium
Chloride Hexahydrate (Absorption/Desorption Process)
As shown in FIG. 5, CaCl.sub.2 can be used for drying HCl. In fact,
CaCl.sub.2 can be used for absorbing water contained into HCl. In
such a case, CaCl.sub.2 is converted into its hexachloride form
(CaCl.sub.2.6H.sub.2O) and one saturated system is eventually
switched into regeneration mode where hot air recovered from
calcination off gas of alumina and magnesium oxide spray roasting
is introduced to regenerate the fixed bed. Alternatively, other
absorbing agent such as LiCl can be used instead of CaCl.sub.2.
Such an ion/exchange type process can be seen in FIG. 4 and the
cycle can be inversed to switch from one column to another one.
The person skilled in the art would understand that the processes
described in examples 3 and 4 can be used in various different
manners. For example, these processes can be combined with the
various processes presented in the present disclosure. For example,
such purifications techniques can be integrated to the processes
shown in FIG. 1, 3 or 6. For example, these techniques can be used
downstream of at least one of step chosen from steps 5, 6, 8, 9, 10
and 11 (see FIGS. 1 and 3). They can also be used downstream of
step 4 and/or step 7. They can also be used downstream of at least
one of step chosen from steps 104 to 111 (see FIG. 6)
EXAMPLE 5
Preparation of Alumina and Various Other Products
This example was carried out by using a process as represented in
FIGS. 6 and 7. It should be noted that the processes represented in
FIGS. 6 and 7 differ only by the fact that FIG. 7 show to
additional stages i.e. stages 112 and 113.
Raw Material Preparation
Raw material, clay for example, was processed in a secondary
crusher in the clay preparation plant 101. Dry milling and
classifying occurs on a dry basis in vertical roller mills (for
example Fuller-Loesche LM 30.41). The clay preparation 101 included
three roller mills; two running at a capacity of approximately
160-180 tph and one on standby. Raw material, if required, can be
reduced to 85% less than 63 microns. Processed material was then
stored in homogenization silos before being fed to the acid
leaching plant 102. Below in Table 1 are shown results obtained
during stage 101. If the ore contains the fluorine element, a
special treatment can be applied before carrying out the 102 stage.
In presence of hydrochloric acid, fluorine can produce hydrofluoric
acid. This acid is extremely corrosive and damaging for human
health. Thus, before leaching 102, an optional treatment fluorine
separation 112 can be done. Stage 112 can comprise treating the
processed material coming from stage 101 with an acid in a
pre-leaching treatment so as to remove hydrofluoric acid.
Therefore, depending on the composition of the raw material, a
fluorine separation stage 112 (or pre-leaching stage 112) can be
carried out.
TABLE-US-00001 TABLE 1 Clay preparation Rate 290 tph Composition
feed SiO.sub.2: 50.9% (main constituents) Al.sub.2O.sub.3: 24.0%
Fe.sub.2O.sub.3: 8.51% CaO: 0.48% MgO: 1.33% Na.sub.2O: 1.06%
K.sub.2O: 2.86% MnO: 0.16% Cr.sub.2O.sub.3: 0.01% TiO.sub.2: 0.85%
P.sub.2O.sub.5: 0.145% SrO: 0.015% BaO: 0.05% V.sub.2O.sub.5
0.0321% Other 9.63% (including H.sub.2O and REE): Obtained particle
size 85% <63 .mu.m Residual moisture 0.5-0.7% Yield 99.5%
min
Acid Leaching
Next, acid leaching 102 was performed semi-continuously in an 80
m.sup.3 glass-lined reactor. Semi-continuous mode comprises
replacing reacted acid 1/3 in the reaction period with higher
concentration regenerated acid, which greatly improves reaction
kinetics. The reactor arrangement comprises for example, a series
of three reactors.
Leaching was performed at high temperature and pressure (about 160
to about 195.degree. C. and pressures of about 5 to about 8 barg)
for a fixed period of time. Reaction time was a function of the
reaction extent targeted (98% for Al.sub.2O.sub.3), leaching mode,
acid strength, and temperature/pressure applied.
Spent acid recovered out of the acid leaching 102 was then filtered
103 from unreacted silica and titanium dioxide and washed through
an automated filter press where all free HCl and chloride are
recovered. This allows, for example, a maximum quantity of about 30
ppm SiO.sub.2 going into spent liquor. Cleaned silica at a
concentration of .apprxeq.96%+SiO.sub.2 is then produced. Various
options are possible at that point. For example, the 96% silica can
undergo final neutralization through caustic bath, cleaning, and
then bricketing before storage. According to another example, the
silica purified by adding another leaching step followed by a solid
separation step that ensures TiO.sub.2 removal (see stage 113 in
FIG. 7). In that specific case, high purity silica 99.5%+ is
produced. In stage 113, titanium and silicium can be separated from
one another in various manners. For example, the solid obtained
from stage 103 can be leached in the presence of MgCl.sub.2 at a
temperature below 90 or 80.degree. C. and at low acid
concentration. For example, acid concentration can be below 25 or
20%. The acid can be HCl or H.sub.2SO.sub.4. In such a case,
titanium remains soluble after such a leaching while titanium is
still in a solid form. These solid and liquid obtained after stage
113 are thus separated to provide eventually TiO.sub.2 and
SiO.sub.2. Water input and flow for silica cleaning is in a ratio
of 1:1 (silica/water) (150 t/h SiO.sub.2/150 t/h H.sub.2O), but
comprises of wash water circulation in closed loop in the process
and limited amount of process water for final cleaning of the
silica and recovery of all chlorides and free HCl generated at the
leaching stage. Below in Table 2 are shown results obtained during
stage 102.
TABLE-US-00002 TABLE 2 Acid Leaching Equivalent solid feed rate
259.6 tph Operation mode Semi-continuous Acid to clay ratio 3.10 @
23% wt (Equivalent to 3.35 with semi-continuous at 18.0% wt)
Regenerated acid 18.0-32.0% concentration Operating temperature
150-155.degree. C. (Pilot) 165-200.degree. C. (Plant) MAWP 120 psig
Typical chemical Fe.sub.2O.sub.3 + 6 HCl .fwdarw. 2 FeCl.sub.3 +
3H.sub.2O reactions Al.sub.2O.sub.3 + 6 HCl .fwdarw. 2 AlCl.sub.3 +
3 H.sub.2O MgO + 2 HCl .fwdarw. MgCl.sub.2 + H.sub.2O K.sub.2O + 2
HCl .fwdarw. 2 KCl + H.sub.2O Re.sub.2O.sub.3 + 6 HCl .fwdarw. 2
ReCl.sub.3 + 3H.sub.2O Spent acid flow to 600-1100 m.sup.3/h
crystallization Practical chemical FeCl.sub.3 4.33% composition
after step FeCl.sub.2 0.19% 102 without solid (SiO.sub.2)
AlCl.sub.3 16.6% MgCl.sub.2 0.82% NaCl 1.1% KCl 1.2% CaCl.sub.2
0.26% Extraction yields Iron 100% Al.sub.2O.sub.3 98% SiO.sub.2
Recovery 99.997%
AlCl.sub.3 Crystallization
Spent acid, with an aluminum chloride content of about 20 to about
30%, was then processed in the crystallization stage 104. Dry and
highly concentrated HCl (>90% wt.) in gas phase was sparged in a
two-stage crystallization reactor, which allows the crystallization
of aluminum chloride hexahydrate.
The flow rate of acid through these reactors is about 600 to about
675 m.sup.3/h and the reactor was maintained at about 50 to about
60.degree. C. during this highly exothermic reaction. Heat was
recovered and exchanged to the acid purification 107 part of the
plant thus ensuring proper heat transfer and minimizing heat
consumption of the plant. Aluminum chloride solubility decreases
rapidly, compared to other elements, with the increase in
concentration of free HCl in the crystallization reactor. The
concentration of AlCl.sub.3 for precipitation/crystallization was
about 30%
The HCl concentration during crystallization was thus about 30 to
about 32% wt.
The aqueous solution from the crystallization stage 104 was then
submitted to the hydrothermal acid recovery plant 105, while the
crystals are processed through the decomposition/calcination stage
in the calcination plant 106.
A one-step crystallization stage or a multi-step crystallization
stage can be done. For example, a two-steps crystallization stage
can be carried out.
Below in Tables 3A and 3B are shown results obtained during stage
104.
TABLE-US-00003 TABLE 3A Aluminum chloride crystallization Number of
crystallization 2 steps Operating temperature 50-60.degree. C.
Sparging HCl concentration 90% (gaseous) Typical chemicals formed
AlCl.sub.3.cndot.6H.sub.2O (s) Metal chlorides (aq)
AlCl.sub.3.cndot.6H.sub.2O residual <5% (practical); 8%
TABLE-US-00004 TABLE 3B Typical crystals composition main
constituents obtained at pilot scale and feeding calcination
Component Weight distribution (%) AlCl.sub.3.cndot.6H.sub.2O 99.978
BaCl.sub.2.cndot.2H.sub.2O 0.0000 CaCl.sub.2.cndot.6H.sub.2O 0.0009
CrCl.sub.4 0.0022 CuCl.sub.2.cndot.2H.sub.2O 0.0000
FeCl.sub.3.cndot.6H.sub.2O 0.0019 KCl 0.0063
MgCl.sub.2.cndot.6H.sub.2O 0.0093 MnCl.sub.2.cndot.4H.sub.2O 0.0011
NaCl 0.0021 SiCl.sub.4 0.0004 SrCl.sub.2.cndot.6H.sub.2O 0.0000
TiCl.sub.4 0.0001 VCl.sub.4 0.0000 Free Cl.sup.- 0.0000
Calcination and Hydrothermal Acid Recovery
The calcination 106 comprises the use of a two-stage circulating
fluid bed (CFB) with preheating systems. The preheating system can
comprise a plasma torch to heat up steam to process. It processes
crystals in the decomposition/calcination stage. The majority of
the hydrochloric acid was released in the first stage which was
operated at a temperature of about 350.degree. C., while the second
stage performs the calcination itself. Acid from both stages (about
66 to about 68% of the recovered acid from the processes) was then
recovered and sent to either to the acid leaching 102 or to the
acid purification 107. In the second reactor, which was operated at
a temperature of about 930.degree. C., acid was recovered through
the condensation and absorption into two columns using mainly wash
water from the acid leaching sector 102. Latent heat from this
sector was recovered at the same time as large amounts of water,
which limits net water input.
In the iron oxides productions and acid recovery 105 system, which
comprises, aqueous solution from the crystallization 104 first
undergoes a pre-concentration stage followed by processing in the
hydrolyzer reactor. Here, hematite was produced during low
temperature processing (about 165.degree. C.). A recirculation loop
was then taken from the hydrolyzer and is recirculated to the
pre-concentrator, allowing the concentration of REE, Mg, K, and
other elements. This recirculation loop, allows rare earth element
chlorides and/or rare metal chlorides and various metal chlorides
concentration to increase without having these products
precipitating with hematite up to a certain extent.
Depending on acid balance in the plant, recovered acid is sent
either directly to the 102 or 107 stage. Table 4 shows results
obtained in stage 105.
TABLE-US-00005 TABLE 4 Hydrothermal acid recovery Flowrate from
crystallization to 592 m.sup.3/h (design) HARP 600 m.sup.3/h
(design) Operating hydrolyser 155-170.degree. C. temperature
Regenerated acid concentration 27.4% Regenerated acid flowrate
205.2 tph HCl Hematite total production rate 24 TPH (design) HCl
recovery >99.8% Reflux (recirculation loop) rate in 56 tph
between hydrolyzer and pre- concentrator Rare earth element
chlorides .apprxeq.12.8 t/h and/or rare metal chlorides rate in
recirculation loop Hematite quality obtained and/or projected
Fe.sub.2O.sub.3 purity >99.5% Hydrolysable chlorides <0.2%
Moisture Max 20% after filtration PSD 25-35 microns Density (bulk)
2-3 kg/l Typical chemical reaction in stage 105 2FeCl.sub.3 +
3H.sub.2O .fwdarw. Fe.sub.2O.sub.3 + 6HCl 155-170.degree. C.
Table 5 shows results obtained in stage 106.
TABLE-US-00006 TABLE 5 Calcination Plant 106 Process
characteristics: Two-stage circulating fluid bed (CFB) with
pre-heating system Two-stage hydrochloric acid regeneration
Production rate (practical) About 66 tph CFB feed rate 371 tph
Typical chemical reaction occurring 2(AlCl.sub.3.cndot.6H.sub.2O) +
Energy .fwdarw. Al.sub.2O.sub.3 + 6HCl + 9H.sub.2O Typical alumina
chemical composition obtained from aluminum chloride hexahydrate
crystals being fed to calcination Component Weight distribution (%)
Al.sub.2O.sub.3 99.938 Fe.sub.2O.sub.3 0.0033 SiO.sub.2 0.0032
Cr.sub.2O.sub.3 0.0063 V.sub.2O.sub.5 0.0077 Na 0.0190 MgO 0.0090
P.sub.2O.sub.5 0.0039 K 0.0053 Ca 0.0020 MnO 0.0002 Free Cl.sup.-
Undetectable
Rare Earth Elements and Rare Metals Extractions
The stream that was taken out of 105 recirculation then was treated
for rare earth elements and are metals extraction 108, in which the
reduction of the remaining iron back to iron 2 (Fe.sup.2+),
followed by a series of solvent extraction stages, was performed.
The reactants were oxalic acid, NaOH, DEHPA
(Di-(2-ethylhexyl)phosphoric acid) and TBP (tri-n-butyl phosphate)
organic solution, kerosene, and HCl were used to convert rare earth
element chlorides and rare metals chlorides to hydroxides.
Countercurrent organic solvent with stripping of solution using HCl
before proceeding to specific calcination from the rare earth
elements and rare metals in form of hydroxide and conversion to
high purity individual oxides. An ion exchange technique is also
capable of achieving same results as polytrimethylen terephtalate
(PET) membrane.
Iron powder from 105, or scrap metal as FeO, can be used at a rate
dependent on Fe.sup.3+ concentration in the mother liquor. HCl
(100% wt) at the rate of 1 tph can be required as the stripped
solution in REE Solvent Extraction (SX) separation and re-leaching
of rare earth elements and/or rare metals oxalates.
Water of very high quality, demineralized or nano, at the rate of
100 tph was added to the strip solution and washing of
precipitates.
Oxalic acid as di-hydrate at a rate of 0.2 tph was added and
contributes to the rare earth elements and rare metals oxalates
precipitation. NaOH or MgOH at a rate of 0.5 tph can be used as a
neutralization agent.
DEHPA SX organic solution at the rate of 500 g/h was used as active
reagent in rare earth elements separation while TBP SX organic
solution at the rate of 5 kg/h is used as the active reagent for
gallium recovery and yttrium separation. Finally, a kerosene
diluent was used at the rate of approximately 2 kg/h in all SX
section. Calcination occurs in an electric rotary furnace via
indirect heating to convert contents to REE.sub.2O.sub.3 (oxides
form) and maintain product purity.
Results of various tests made regarding stage 108 are shown in
Table 6.
One line divided in subsections (5) to isolate the following
elements using solvent extraction: Ga.sub.2O.sub.3 Y.sub.2O.sub.3
Sc.sub.2O.sub.3 Eu.sub.2O.sub.3+Er.sub.2O.sub.3+Dy.sub.2O.sub.3
Ce.sub.2O.sub.3+Nd.sub.2O.sub.3+Pr.sub.2O.sub.3
TABLE-US-00007 Equivalent output earths oxides 166.14 kg/h
Projected production as per pilot testing results Incoming Final
extraction Feed (kg/h) individual (kg/h) Ga.sub.2O.sub.3 15.66
11.98 Sc.sub.2O.sub.3 9.06 8.11 Y.sub.2O.sub.3 22.56 20.22
La.sub.2O.sub.3 32.24 25.67 Ce.sub.2O.sub.3 61.37 51.82
Pr.sub.2O.sub.3 8.08 6.18 Nd.sub.2O.sub.3 30.3 27.24
Sm.sub.2O.sub.3 5.7 4.51 Eu.sub.2O.sub.3 1.06 0.95 Gd.sub.2O.sub.3
4.5 4.06 Dy.sub.2O.sub.3 3.9 3.55 Er.sub.2O.sub.3 2.1 1.86 Total
196.55 166.14 Global yield: 84.53%
Alternatively, stage 108 can be carried out as described in
PCT/CA2012/000253 and/or PCT/CA2012000419.
The solution after stages 108 and 109 contained mainly MgCl.sub.2,
NaCl, KCl, CaCl.sub.2, FeCl.sub.2/FeCl.sub.3, and AlCl.sub.3
(traces), and then follows stage 111 Na, K, Ca that follows the MgO
can be extracted in stage 110 by crystallization in a specific
order; Na first, followed by K, and then Ca. This technique can be
employed for example in the Israeli Dead Sea salt processing plant
to produce MgO and remove alkali from the raw material.
HCl Regeneration
Alkali (Na, K), once crystallized, was sent and processed in the
alkali hydrochloric acid regeneration plant 110 for recovering
highly concentrated hydrochloric acid (HCl). The process chosen for
the conversion can generate value-added products
Various options are available to convert NaCl and KCl with intent
of recovering HCl. One example can be to contact them with highly
concentrated sulfuric acid (H.sub.2SO.sub.4), which generates
sodium sulphate (Na.sub.2SO.sub.4) and potassium sulfate
(K.sub.2SO.sub.4), respectively, and regenerates HCl at a
concentration above 90% wt. Another example, is the use of a sodium
and potassium chloride brine solution as the feed material to
adapted small chlor-alkali electrolysis cells. In this latter case,
common bases (NaOH and KOH) and bleach (NaOCl and KOCl) are
produced. The electrolysis of both NaCl and KCl brine is done in
different cells where the current is adjusted to meet the required
chemical reaction. In both cases, it is a two-step process in which
the brine is submitted to high current and base (NaOH or KOH) is
produced with chlorine (Cl.sub.2) and hydrogen (H.sub.2). H.sub.2
and Cl.sub.2 are then submitted to a common flame where highly
concentrated acid in gas (100% wt.) phase is produced and can be
used directly in the crystallization stage 104, or to
crystallization stages requiring dry highly concentrated acid.
Magnesium Oxide
The reduced flow, which was substantially free of most elements
(for example AlCl.sub.3, FeCl.sub.3, REE-Cl, NaCl, KCl) and rich in
MgCl.sub.2, was then submitted to the magnesium oxides plant 111.
In the MgO, pyrohydrolysis of MgCl.sub.2 and any other leftover
impurities were converted into oxide while regenerating acid. The
first step was a pre-evaporator/crystallizer stage in which calcium
is removed and converted into gypsum (CaSO.sub.4.2H.sub.2O) by a
simple chemical reaction with sulfuric acid, for which separation
of MgO is required. This increases the capacity of MgO roasting and
also energy consumption slightly, while substantially recovering
HCl. The next step was the specific pyrohydrolysis of MgO
concentrated solution by spray roasting. Two (2) main products were
generated; MgO that was further treated and HCl (about 18% wt.),
which was either recycled back to the upstream leaching stage 102
or to the hydrochloric acid purification plant (107 The MgO-product
derived from the spray roaster can require further washing,
purification, and finally calcining depending on the quality
targeted. The purification and calcining can comprise a
washing-hydration step and standard calcining step.
The MgO from the spray roaster is highly chemically active and was
directly charged into a water tank where it reacts with water to
form magnesium hydroxide, which has poor solubility in water. The
remaining traces of chlorides, like MgCl.sub.2, NaCl, dissolved in
water. The Mg(OH).sub.2 suspension, after settling in a thickener,
was forwarded to vacuum drum filters, which remove the remaining
water. The cleaned Mg(OH).sub.2 is then forwarded into a
calcination reactor where it is exposed to high temperatures in a
vertical multi-stage furnace. Water from hydration is released and
allows the transformation of the Mg(OH).sub.2 to MgO and water. At
this point, the magnesium oxide was of high purity (>99%).
HCl Purification
The hydrochloric acid purification stage 107 is effective for
purifying HCl regenerated from different sectors (for example 105,
106, 111) and to increase its purity for crystallization, whereas
dry highly concentrated acid (>90% wt.) can be used as the
sparging agent. Stage 107 also allowed for controlling the
concentration of the acid going back to stage 102 (about 22 to
about 32% wt.) and allows total acid and water balance. Total plant
water balance is performed mainly by reusing wash water as
absorption medium, as quench agent or as dissolution medium at the
crystallization stages
For example, purification can be carried out by means of a membrane
distillation process. The membrane distillation process applied
here occurs when two aqueous liquids with different temperatures
are separated through a hydrophobic membrane. The driving force of
the process was supplied by the partial pressure vapour difference
caused by the temperature gradient between these solutions. Vapour
travels from the warm to the cold side. Without wishing to be bound
to such a theory, the separation mechanism was based on the
vapour/liquid equilibrium of the HCl/water liquid mixture.
Practical application of such a technology has been applied to
HCl/water, H.sub.2SO.sub.4/water systems and also on large
commercial scales on aqueous solution of sodium chloride with the
purpose of obtaining potable water from seawater and nano water
production. Therefore membrane distillation was a separation
process based on evaporation through a porous hydrophobic membrane.
The process was performed at about 60.degree. C. and was effective
to recover heat from the 104 and 102 stage with an internal water
circulation loop, in order to maintain a constant incoming
temperature to the membranes. For example, eight membranes of
300,000 m.sup.2 equivalent surface area can be used per membrane to
obtain a concentration of HCl well above the azeotropic point (i.e.
>36%) of the .apprxeq.750 m.sup.3/h and final 90% concentration
is then obtained through pressure distillation (rectification
column).
Purification of HCl by processing thus regenerated acid through
hydrophobic membrane and separating water from HCl; therefore
increasing HCl concentration up to about 36% (above azeotropic
point) and therefore allowing with a single stage of rectification
through a pressure stripping column to obtain >90% in gaseous
phase, for crystallization stage (sparging); and therefore
controlling acid concentration into crystallization stages up to
30-35%.sub.(aq).
As indicated stage 107 was operated at about 60.degree. C. and heat
input provided by heat recovery from stages 102 to 110.
Rectification column was operated at about 140.degree. C. in the
reboiler part. Net energy requirement was neutral (negative in fact
at -3.5 Gj/t Al.sub.2O.sub.3) since both systems were in
equilibrium and in balance.
For example, the acid purification can be carried out by using
adsorption technology over an activated alumina bed. In continuous
mode, at least two adsorption columns are required to achieve
either adsorption in one of them and regeneration in the other one.
Regeneration can be performed by feeding in counter-current a hot
or depressurized gas. This technology will result in a purified gas
at 100% wt.
For example, the acid purification can be made by using calcium
chloride as entrainer of water. A lean hydrochloric acid solution
is contacted with a strong calcium chloride solution through a
column. The water is then removed from the hydrochloric acid
solution and 99.9% gaseous HCl comes out of the process. Cooling
water and cryogenic coolant is used to condense water traces in the
HCl. The weak CaCl.sub.2 solution is concentrated by an evaporator
that ensures the recuperation of calcium chloride. Depending on the
impurities in the incoming HCl solution feed to the column, some
metals can contaminate the calcium chloride concentrated solution.
A precipitation with Ca(OH).sub.2 and a filtration allows the
removal of those impurities. The column can operate for example at
0.5 barg. This technology can allow for the recuperation of 98% of
the HCl.
Table 7 shows the results obtained concerning the process shown in
FIG. 6.
TABLE-US-00008 Composition Stage 101 Stage 102 Stage 106 Stage 105
MgO Stage 107 Stage 108 TOTAL PRODUCED (% wt) Yield (%) Yield (%)
Yield (%) Yield (%) tpy Yield (%) Yield (%) Yield (%) Yield (%)
Main constituents SiO.sub.2 -- 99.997% -- -- -- -- -- -- 99.997% Al
-- 98.02% 95.03% -- -- -- -- -- 95.03% Fe -- 100.00% -- 92.65% --
-- -- -- 92.65% Mg -- 99.998% -- -- 29,756 92.64% -- -- 92.64% Ca
-- 99.998% -- -- -- -- -- -- 98.28% Na -- 99.998% -- -- -- -- -- --
92.76% K -- 100.00% -- -- -- -- -- -- 93.97% Others incl. H.sub.2O
-- -- -- -- -- -- -- -- RE/RM -- 99.80% -- 92.32% -- -- -- 84.67%
84.67% By-Products NaOH -- -- -- -- 68,556 -- -- -- -- NaOCl -- --
-- -- 9,269 -- -- -- -- KOH -- -- -- -- 73,211 -- -- -- -- KOCl --
-- -- -- 9,586 -- -- -- -- CaSO.sub.4 -- -- -- -- 46,837 -- -- --
-- Reactants H.sub.2SO.sub.4(*) -- -- -- -- 19,204 -- -- -- --
Fresh HCl M-UP -- -- -- -- -- -- 99.75% -- 99.75% Total -- 98.55%
95.03% 256,419 92.64% 99.75% 84.67%
Tables 8 to 26 show results obtained concerning the products made
in accordance with the process shown in FIG. 6 in comparison with
standard of the industry.
TABLE-US-00009 TABLE 8 Chemical composition of obtained alumina
Element % Weight Standard used in industry Al.sub.2O.sub.3 99.938
98.35 min Fe.sub.2O.sub.3 0.0033 0.0100 SiO.sub.2 0.0032 0.0150
TiO.sub.2 0.0003 0.0030 V.sub.2O.sub.5 0.0008 0.0020 ZnO 0.0005
0.0030 Cr.sub.2O.sub.3 0.0003 N/A MgO 0.0090 N/A MnO 0.0002 N/A
P.sub.2O.sub.5 0.0039 0.0010 Cu 0.0030 N/A Ca 0.0020 0.0030 Na
0.0190 0.4000 K 0.0053 0.0150 Li 0.0009 N/A Ba <0.00001 0.0000
Th <0.000001 0.0000 U <0.000001 0.0000 Free Cl.sup.- Not
detectable 0.0000 LOI <1.0000 <1.0000
TABLE-US-00010 TABLE 9 Physical properties of obtained alumina
Property Orbite Alumina Standard used in industry PSD < 20 .mu.m
5-10% N/A PSD < 45 .mu.m 10-12% <10% PSD > 75 .mu.m 50-60%
N/A SSA (m.sup.2/g) 60-85.sup. 60-80 Att. Index 10-12% <10%
.alpha. Al.sub.2O.sub.3 2-5% <7-9%
TABLE-US-00011 TABLE 10 Chemical composition of obtained hematite
Element % Weight Fe.sub.2O.sub.3 >99.5% Hydrolysable elements
<0.2%
TABLE-US-00012 TABLE 11 Physical properties of obtained hematite*
Property Orbite hematite PSD.sub.mean 25-35 .mu.m Density (bulk)
2000-3000 kg/m.sup.3 Humidity after filtration <10% *Material
can be produced as brickets
TABLE-US-00013 TABLE 12 Chemical composition of obtained silica
Element % Weight SiO.sub.2 >99.7 Al.sub.2O.sub.3 <0.25% MgO
.apprxeq.0.1% Fe.sub.2O.sub.3 .apprxeq.0.1% CaO .apprxeq.0.01%
Na.sub.2O <0.1% K.sub.2O <0.1% Note: Product may have
unbleached cellulose fiber filter aid. Cellulose wood flour.
TABLE-US-00014 TABLE 13 Physical properties of obtained silica
Property Orbite silica PSD.sub.mean 10-20 .mu.m Specific surface
area 34 m.sup.2/g Density (bulk) 2000-2500 kg/m.sup.3 Humidity
after filtration <40%
TABLE-US-00015 TABLE 14 Purity of obtained rare earth element
oxides Element Purity (%) Ga.sub.2O.sub.3 >99% Sc.sub.2O.sub.3
Y.sub.2O.sub.3 La.sub.2O.sub.3 Ce.sub.2O.sub.3 Pr.sub.2O.sub.3
Nd.sub.2O.sub.3 Sm.sub.2O.sub.3 Eu.sub.2O.sub.3 Gd.sub.2O.sub.3
Dy.sub.2O.sub.3 Er.sub.2O.sub.3 Physical properties of obtained
REE-O/RM-O Property Orbite REE-O/RM-O PSD.sub.mean 2-30 .mu.m
Density 5500-13000 kg/m.sup.3 LOI <1%
TABLE-US-00016 TABLE 15 Chemical composition of obtained MgO
Element Typical Specification MgO 99.0.sup.+ 98.35 min CaO 0.0020
0.83 SiO.sub.2 0.0000 0.20 max B.sub.2O.sub.3 0.0000 0.02 max
Al.sub.2O.sub.3 0.0300 0.12 max Fe.sub.2O.sub.3 0.0160 0.57 max
MnO.sub.2 <0.14 0.14 max LOI 0.7% <1%
TABLE-US-00017 TABLE 16 Physical properties of obtained MgO
Property Orbite MgO PSD.sub.mean 10 .mu.m Density N/A LOI 650
kg/m.sup.3
TABLE-US-00018 TABLE 17 Chemical composition of obtained NaOH
Element % Weight Sodium hydroxide 32% Water 68%
TABLE-US-00019 TABLE 18 Physical properties of obtained NaOH
Property Sodium hydroxide (NaOH) Physical state Liquid Vapour
pressure 14 mmHg Viscosity >1 Boiling point 100.degree. C.
Melting point 0.degree. C. Specific gravity 1.0
TABLE-US-00020 TABLE 19 Chemical composition of obtained sodium
hypochlorite (bleach) Element % Weight Sodium hypochlorite 12%
Sodium hydroxide <1% Water >80%
TABLE-US-00021 TABLE 20 Physical properties of obtained NaOCl
Property Sodium hypochlorite (NaOCl) Physical state Liquid Vapour
pressure 1.6 kPa Viscosity N/A Boiling point 100.degree. C. Melting
point -3.degree. C. Specific gravity 1.2
TABLE-US-00022 TABLE 21 Chemical composition of obtained potassium
hydroxide Element % Weight Potassium hydroxide 32% Water 68%
TABLE-US-00023 TABLE 22 Physical properties of obtained potassium
hydroxide Property KOH Physical state Liquid Vapour pressure 17.5
mmHg Viscosity N/A Boiling point 100.degree. C. Melting point N/A
Specific gravity 1.18
TABLE-US-00024 TABLE 23 Chemical composition of obtained potassium
hypochlorite (KOCl) Element % Weight Potassium hypochlorite 12%
Potassium hydroxide <1% Water >80%
TABLE-US-00025 TABLE 24 Physical properties of obtained potassium
hypochlorite Property KOCl Physical state Liquid Vapour pressure
N/A Viscosity N/A Boiling point 103.degree. C. Melting point N/A
Specific gravity >1.0
TABLE-US-00026 TABLE 25 Chemical composition of obtained calcium
sulphate dihydrate Element % Weight Calcium sulphate dihydrate
100%
TABLE-US-00027 TABLE 26 Physical properties of obtained calcium
sulphate dihydrate Property Orbite CaSO.sub.4.cndot.2H.sub.2O
Physical state Solid Specific gravity 2.32
In order to demonstrate the versatility of the processes of the
present disclosure, several other tests have been made so as to
shown that these processes can be applied to various sources of
starting material.
EXAMPLE 6
Another starting material has been used for preparing acidic
compositions comprising various components. In fact, a material
that is a concentrate of rare earth elements and rare metals
(particularly rich in zirconium) has been tested. Table 27 shows
the results of the leaching carried out on such a starting material
using a similar process as shown in FIGS. 1, 3, 6 and 7 and as
detailed in Examples 1, 2 and 5. It can thus be inferred from the
results shown in Table 27 that the various components present in
the leaching (various metals such as aluminum, iron, magnesium as
well as rare earth elements and rare metals) can be extracted from
the obtained leaching composition and that they can eventually be
isolated by the processes of the present disclosure such as, for
example, those presented in Examples 1, 2 and 5.
EXAMPLE 7
Other tests have been made in a similar manner as described in
Example 6. In the present example, carbonatite has been used as a
starting material. (see Table 28 below).
TABLE-US-00028 TABLE 27 Tests made on a zirconium rich material.
Composition Average measure and/ measured Extraction O All Raw or
evaluated for testing rate measured Orbite process material (% wt.)
(% wt .) (ALP) (%) recovery (%) Al.sub.2O.sub.3 6.12 6.12 89.65
86.97 Fe.sub.2O.sub.3 15.80 15.80 99.50 97.51 SiO.sub.2 36.00 36.00
0.000 99.997 MgO 3.08 3.08 99.75 92.66 Na.sub.2O 1.13 1.13 99.50
99.50 K.sub.2O 2.12 2.12 99.50 99.50 CaO 6.10 6.10 99.50 99.00 S
total 0.22 0.22 100.00 F 1.98 1.98 99.50 99.00 TiO.sub.2 0.13 0.13
0.000 99.03 V.sub.2O.sub.5 0.00 0.00 98.00 96.04 P.sub.2O.sub.5
1.10 1.10 98.00 96.04 MnO 0.43 0.43 98.00 96.04 ZrO.sub.2 12.43
12.43 22.70 20.43 Cr.sub.2O.sub.3 0.00 0.00 0.00 0.00
Ce.sub.2O.sub.3 3.05 3.045 97.31 92.98 La.sub.2O.sub.3 1.34 1.337
99.55 92.68 Nd.sub.2O.sub.3 1.55 1.551 98.40 94.79 Pr.sub.2O.sub.3
0.37 0.375 99.75 97.52 Sm.sub.2O.sub.3 0.15 0.151 88.75 84.80
Dy.sub.2O.sub.3 0.09 0.089 80.35 76.77 Er.sub.2O.sub.3 0.03 0.030
72.60 69.37 Eu.sub.2O.sub.3 0.03 0.027 85.57 81.76 Gd.sub.2O.sub.3
0.21 0.205 82.85 79.16 Ho.sub.2O.sub.3 0.01 0.013 77.10 73.67
Lu.sub.2O.sub.3 0.00 0.003 60.15 57.47 Tb.sub.2O.sub.3 0.02 0.022
78.05 74.58 Th 0.02 0.022 88.10 84.18 Tm.sub.2O.sub.3 0.00 0.004
66.85 63.88 U 0.01 0.014 81.90 78.26 Y.sub.2O.sub.3 0.30 0.300
72.70 69.46 Yb.sub.2O.sub.3 0.02 0.023 62.80 60.01 Ga.sub.2O.sub.3
0.02 0.016 96.90 92.59 Sc.sub.2O.sub.3 0.00 0.003 95.00 90.77 LOI
(inc. 6.122023973 6.12 water)
TABLE-US-00029 TABLE 28 Tests made on carbonatite Composition
Average measure and/ measured Extraction O All Raw or evaluated for
testing rate measured Orbite process material (% wt.) (% wt.) (ALP)
(%) recovery (%) Al.sub.2O.sub.3 0.70 0.70 84.31 81.61
Fe.sub.2O.sub.3 11.22 11.22 94.14 92.15 SiO.sub.2 2.11 2.11 0.00003
99.997 MgO 6.50 6.500 100 96.25 Na.sub.2O 0.07 0.07 92.54 90.55
K.sub.2O 0.18 0.181 37.33 37.33 CaO 16.51 16.51 100 98.00 TiO.sub.2
0.00 0.000 0.00000 100.000 V.sub.2O.sub.5 0.00 0.000 0 100.000
P.sub.2O.sub.5 0.00 0.000 0 100.000 MnO 0.00 0.000 0 100.000
ZrO.sub.2 0.00 0.000 0 100.000 Cr.sub.2O.sub.3 0.00 0.000 0 100.000
Ce.sub.2O.sub.3 1.19 1.195 64.04 61.190 La.sub.2O.sub.3 0.46 0.463
63.86 61.018 Nd.sub.2O.sub.3 0.45 0.448 81.46 77.835
Pr.sub.2O.sub.3 0.14 0.142 67.59 64.582 Sm.sub.2O.sub.3 0.03 0.033
65.32 62.413 Dy.sub.2O.sub.3 0.00 0.000 78.12 74.644
Er.sub.2O.sub.3 0.00 0.000 86.15 82.316 Eu.sub.2O.sub.3 0.01 0.007
66.45 63.493 Gd.sub.2O.sub.3 0.01 0.013 54.46 52.037
Ho.sub.2O.sub.3 0.00 0.000 83.12 79.421 Lu.sub.2O.sub.3 0.00 0.000
88.86 84.906 Tb.sub.2O.sub.3 0.00 0.001 41.42 39.577 Th 0.06 0.065
Tm.sub.2O.sub.3 0.00 0.000 90.70 86.664 U 0.01 0.007 Y.sub.2O.sub.3
0.00 0.000 84.68 80.912 Yb.sub.2O.sub.3 0.00 0.000 85.11 81.323
Ga.sub.2O.sub.3 0.00 0.000 0 0.000 Sc.sub.2O.sub.3 0.00 0.000 0
0.000 LOI (inc. 60.33 water)
It can thus be inferred from the results shown in Table 28 that the
various metals, rare earth elements and rare metals extracted
present in the obtained leaching composition can eventually be
isolated by the processes of the present disclosure such as, for
example, those presented in Examples 1, 2 and 5.
EXAMPLE 8
Test have been made for using fly ash as starting material. The
results are shown below in Tables 29, 30 and 31.
TABLE-US-00030 TABLE 29 Leaching conditions for fly ash Leaching
Operating Conditions Processing Reactor Pressure Temperature Time
Acid Ratio Volume 75-80 psi 150-165.degree. C. 420 Stoichiom- 16
gallons minutes etry + 30%
TABLE-US-00031 TABLE 30 Fly ash used Fly Ash Masse In 2600 Masse
Out 302 % H2O 30%
TABLE-US-00032 TABLE 31 Results - leaching of fly ash Recovery
Yield % Al K Na Fe Ca Si Initial % 8.02 1.21 0.42 8.27 1.65 13.9
compound kg 208.52 31.45 10.92 215.02 42.9 361.4 Cake % 9.15 1.15
0.26 1.75 0.3 36.9 kg 19.3431 2.4311 0.54964 3.6995 0.6342 78.0066
% recovery 90.72% 92.27% 94.97% 98.28% 98.52% 78.42% * 0% MgO
initially
It can thus be seen that fly ash has been successfully leached with
HCl, thereby allowing for good yields with respect to the recovery
of the various components present in Fly ash. These various
products or components present in the obtained leachate can thus be
all isolated and eventually transformed as previously indicated in
the processes of the present disclosure. The obtained leachate can
then be treated as described in the processes of the present
disclosure. The leaching of example 8 can be considered, for
example, as the leaching 2 of FIG. 1 or FIG. 3; the leaching 102 of
FIG. 6 or FIG. 7, etc. For example, the leachate obtained in
Example 8 can then be treated as shown in FIGS. 1, 3, 6 and 7.
EXAMPLE 9
Other tests have been made for using another alternative source of
fly ash. A similar process was used. The initial measured
conditions were:
TABLE-US-00033 TABLE 32 Fly Ash initial composition Element
Composition measured (% wt) SiO.sub.2 29.73 Al.sub.2O.sub.3 15.15
Fe.sub.2O.sub.3 11.82 CaO 2.31 Na.sub.2O 0.57 K.sub.2O 1.46
The samples were leached in batch mode at 75 psig (150.degree. C.)
for a 6 hours duration at stoechiometry +5% excess Hcl (20%
wt).
The following extraction yields were measured at the leaching
stage:
TABLE-US-00034 TABLE 33 Leaching extraction yield measured Raw
element Extraction measured (% wt) Al.sub.2O.sub.3 96.1
Fe.sub.2O.sub.3 98.5 N 95.7 Na.sub.2O K.sub.2O 93.4 CaO 98.7
After processing through main steps of process (see for example
FIG. 6), the following yields were measured.
TABLE-US-00035 TABLE 34 Global recovery yield Element Global
recovery (% wt) Al.sub.2O.sub.3 93.4 Fe.sub.2O.sub.3 96.5 SiO.sub.2
99.99 No2.sub.2O 93.7 K.sub.2O 93.4 CaO 96.8
Main characteristics of produced alumina were: Chemical
composition: 99.4%; PSD dp.sub.50: 63 um; .alpha. Al.sub.2O.sub.3:
2%; and Bulk density: 0.63.
EXAMPLE 10
Other tests was performed on another alternative source of material
always using the same process as per previous examples. The initial
composition measured was:
TABLE-US-00036 TABLE 35 Fly Ash initial composition Element
Composition measured (% t wt) SiO.sub.2 44.9 Al.sub.2O.sub.3 22.1
Fe.sub.2O.sub.3 21.0 CaO 4.1 Na.sub.2O 0.7 K.sub.2O 2.4
The samples were leached in hatch mode at 160.degree. C. (80 psig)
for a 6 hours duration at stoichiometry +10% Hcl excess (20%
wt).
The following extraction yields were measured at the leaching
stage.
TABLE-US-00037 TABLE 36 Leaching extraction yield measured Raw
element Extraction measured (% wt) Al.sub.2O.sub.3 97.6
Fe.sub.2O.sub.3 99.5 Na.sub.2O 91.1 K.sub.2O 93.3 CaO 94.9
After processing through main steps of continuous process (see FIG.
6) the following yield were measured:
TABLE-US-00038 TABLE 37 Global recovery yield Element Global
recovery (% wt) Al.sub.2O.sub.3 94.9 Fe.sub.2O.sub.3 97.5 SiO.sub.2
99.99 Na2O 89.1 K.sub.2O 93.3 CaO 93.0
The applicants have now discovered fully integrated and continuous
processes with substantially total hydrochloric acid recovery for
the extraction of alumina and other value added products from
various materials that contain aluminum (clay, bauxite,
aluminosilicate materials, slag, red mud, fly ash etc.) containing
aluminum. In fact, the processes allows for the production of
substantially pure alumina and other value added products purified
such as purified silica, pure hematite, pure other minerals (ex:
magnesium oxide) and rare earth elements products. In addition, the
processes do not require thermal pre-treatment before the acid
leach operation. Acid leach can be carried out using
semi-continuous techniques with high pressure and temperature
conditions and very high regenerated hydrochloric acid
concentration. The processes can also be carried out at atmospheric
pressure. In addition, the processes do not substantially generate
any residues not sellable, thus eliminating harmful residues to
environment like in the case of alkaline processes.
The advantage of the high temperature calcination stage, in
addition for allowing to control the .alpha.-form of alumina
required, can be effective for providing a concentration of
hydrochloric acid in the aqueous form (>38%) that is higher than
the concentration of HCl at the azeotropic point and thus providing
a higher incoming HCl concentration to the leaching stage. The
calcination stage hydrochloric acid network can be interconnected
to two (2) crystallization systems and by pressure regulation
excess HCl can be being absorbed at the highest possible aqueous
concentration. The advantage of having a hexahydrate chloride with
low moisture content (<2%) incoming feed allows for a continuous
basis to recover acid at a concentration that is higher than the
azeotropic concentration. This HCl balance and double usage into
three (3) common parts of the processes and above azeotropic point
is a substantial advance in the art.
Another advantage is when the use is made of the incoming chemistry
(ferric chloride) to the iron oxide and hydrochloric acid recovery
unit where all excess heat load from any calcination part,
pyrohydrolysis and leaching part is being recovered to
preconcentrate the mother liquor in metal chloride, thus allowing,
at very low temperature, the hydrolysis of the ferric chloride in
the form of very pure hematite and the acid regeneration at the
same concentration than at its azeotropic point.
A further major advantage of the processes of the present
disclosure at the ferric chloride hydrolysis step can be the
possibility to concentrate rare earth elements in form of chlorides
at very high concentration within the hydrolyser reactor through an
internal loop between hydrolyzer and crystallization. The advantage
is that the processes of the present disclosure benefit from the
various steps where gradual concentration ratios are applied. Thus,
at this stage, in addition to an internal concentration loop,
having the silica, the aluminum, the iron and having in equilibrium
a solution close to saturation (large amount of water evaporated,
no presence of free hydrochloric acid) allows for taking rare earth
elements and non-hydrolysable elements in parts per million into
the incoming feed and to concentrate them in high percentage
directly at the hydrolyser after ferric chloride removal
Purification of the specific oxides (RE-O) can then be performed
using various techniques when in percentage levels. The advantage
can be doubled here: concentration at very high level of rare earth
elements using integrated process stages and most importantly the
approach prevents from having the main stream (very diluted) of
spent acid after the leaching step with the risk of contaminating
the main aluminum chloride stream and thus affecting yields in
Al.sub.2O.sub.3. Another important improvement of the art can be
that on top of being fully integrated, selective removal of
components allows for the concentration of rare earth elements to
relatively high concentration (percentages).
Another advantage of the processes can be again a selective
crystallization of MgCl.sub.2 through the sparging of HCl from
either the alumina calcination step or the magnesium oxide direct
calcination where in both cases highly concentrated acid both in
gaseous phase or in aqueous form are being generated. As per
aluminum chloride specific crystallization, the direct
interconnection with the calcination reactor, the HCl gas very high
concentration (about 85 to about 95%, about 90 to 95% or about 90%
by weight) allows for exact adjustment in continuous of the
crystallizer based on quality of magnesium oxide targeted. Should
this process step (MgO production or other value added metal oxide)
be required based on incoming process feed chemistry, the rare
earth elements extraction point then be done after this additional
step; the advantage being the extra concentration effect
applied.
The pyrohydrolysis can allow for the final conversion of any
remaining chloride and the production of refined oxides that can be
used (in case of clay as starting material) as a fertilizer and
allowing the processing of large amount of wash water from the
processes with the recovery of hydrochloric acid in close loop at
the azeotropic point for the leaching step. The advantage of this
last step can be related to the fact that it does totally close the
process loop in terms of acid recovery and the insurance that no
residues harmful to the environment are being generated while
processing any type of raw material, as previously described.
A major contribution to the art can be that the proposed fully
integrated processes of the present disclosure are allowing, among
others, the processing of bauxite in an economic way while
generating no red mud or harmful residues. In addition to the fact
of being applicable to other natural of raw materials (any suitable
aluminum-containing material or aluminous ores), the fact of using
hydrochloric acid total recovery and a global concentration that
can be higher than the concentration at the azeotropic point (for
example about 21% to about 38%), the selective extraction of value
added secondary products and compliance (while remaining highly
competitive on transformation cost) with environmental
requirements, represent major advantages in the art.
The processes of the present disclosure can provide fully
continuous and economical solutions that can successfully extract
alumina from various type of materials while providing ultra pure
secondary products of high added value including highly
concentrated rare earth elements and rare metals. The technology
described in the present disclosure can allow for an innovative
amount of total acid recovery and also for a ultra high
concentration of recovered acid. When combing it to the fact that
combined with a semi-continuous leaching approach that favors very
high extraction yields and allows a specific method of
crystallization of the aluminum chloride and concentration of other
value added elements. These processes can also allow for preparing
aluminum with such a produced alumina.
For example, through the type of equipment that can be used (for
example vertical roller mill) and its specific operation, raw
material grinding, drying and classifying can be applicable to
various kinds of material hardness (furnace slag for example),
various types of humidity (up to 30%) and incoming particle sizes.
The particle size established can provide the advantage, at the
leaching stage, of allowing efficient contact between the minerals
and the acid and then allowing faster kinetics of reaction.
Particles size employed can be effective to reduce drastically the
abrasion issue and allows for the use of a simplified
metallurgy/lining when in contact with hydrochloric acid.
A further advantage of the processes of the present disclosure can
be the combined high temperature and high incoming hydrochloric
acid concentration. Combined with a semi continuous operation where
the free HCl driving force can be used systematically, iron and
aluminum extraction yields do respectively reach 100% and 98% in
less than about 40% of the reference time of a basic batch process.
Another advantage of higher HCl concentration than the
concentration at azeotropic point can be the potential of capacity
increase. Again a higher HCl concentration than the concentration
of HCl at the azeotropic point and the semi-continuous approach can
represent a substantial advance in the art.
Another advantage in that technique used for the mother liquor
separation from the silica after the leaching stage countercurrent
wash, can be that band filters provide ultra pure silica with
expected purity exceeding 96%.
The crystallization of AlCl.sub.3 into AlCl.sub.3.6H.sub.2O using
dried, cleaned and highly concentrated gaseous HCl as the sparging
agent can allow for a pure aluminum chloride hexahydrate with only
few parts per million of iron and other impurities. A minimal
number of stages can the be required to allow proper crystal
growth.
The direct interconnection with the calcination of
AlCl.sub.3.6H.sub.2O into Al.sub.2O.sub.3 which can produce very
high concentration of gas allows the exact adjustment in continuous
of the HCl concentration within the crystallizer and thus proper
control of the crystal growth and crystallization process.
It was thus demonstrated that the present disclosure provides fully
integrated processes for the preparation of pure aluminum oxide
using a hydrochloric acid treatment while producing high purity and
high quality products (minerals) and extracting rare earth elements
and rare metals.
While a description was made with particular reference to the
specific embodiments, it will be understood that numerous
modifications thereto will appear to those skilled in the art.
Accordingly, the above description and accompanying drawings should
be taken as specific examples and not in a limiting sense.
* * * * *
References